5488 NP_001070868 M440I not found in SNVbox database
7603 NP_705833 F375C not found in SNVbox database
7745 NP_705833 H551N not found in SNVbox database
8049 NP_705833 I980M not found in SNVbox database
8842 NP_705833 P517L not found in SNVbox database
1093 NP_001070868 K646N not found in SNVbox database
1302 NP_001070868 T98K not found in SNVbox database
1385 NP_705833 W388C not found in SNVbox database
3665 NP_705833 Q72P not found in SNVbox database
4553 NP_001070868 N242K not found in SNVbox database
4614 NP_705833 S916F not found in SNVbox database
4803 NP_001070868 S554P not found in SNVbox database
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr10:52573784 C>A maps to NM_138932.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:7680644 C>A maps to NM_145891.2 S259S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-34-2608-01A-02D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr16:7568162 A>C maps to NM_145891.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:7568384 C>G maps to NM_145891.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:9225293 C>T maps to NM_000014.4 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:9256834 C>T maps to NM_000014.4 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:9242508 G>A maps to NM_000014.4 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr12:9251319 G>C maps to NM_000014.4 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr12:9221439 T>C did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:9262610 G>A maps to NM_000014.4 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr12:9227263 A>G maps to NM_000014.4 Y1216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:9010649 C>G maps to NM_144670.3 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:8994044 C>T maps to NM_144670.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:9000179 A>G maps to NM_144670.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr12:8998721 C>T maps to NM_144670.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:8975786 G>T maps to NM_144670.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:9009778 C>A maps to NM_144670.3 A956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:53715195 T>A maps to NM_015665.5 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:125609518 G>T maps to NM_023928.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:151451951 T>C maps to NM_207365.3 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:12785626 G>A maps to NM_001103170.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr4:170994373 G>A maps to ENST00000509167 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr16:70302212 G>C maps to ENST00000418685 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:44272022 G>T maps to NM_020745.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr17:41108543 C>T maps to NM_001136042.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:57204810 T>G maps to NM_181806.2 S1018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr4:57248729 G>T maps to NM_181806.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr4:57221561 C>A maps to NM_181806.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:105948586 G>A maps to NM_015423.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr11:105962124 T>G maps to NM_015423.2 L205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:105961332 C>A maps to NM_015423.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:121738555 T>A maps to NM_005763.3 K535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr7:121738538 C>A maps to NM_005763.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:121753270 C>G maps to NM_005763.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:35311100 C>T maps to NM_012138.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr16:8862806 G>T maps to NM_001127448.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr16:8829666 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:107651463 G>A maps to NM_005502.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr9:107549167 C>T maps to NM_005502.3 V2098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr9:107581072 A>T maps to NM_005502.3 C1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr9:107602610 C>A maps to NM_005502.3 G335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr9:107645434 C>A maps to NM_005502.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr9:107556764 C>A maps to NM_005502.3 L1803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:107584879 G>A maps to NM_005502.3 R909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:107560722 G>C maps to NM_005502.3 L1700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:107560845 G>A maps to NM_005502.3 I1659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:67181616 C>T did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr17:67170798 G>A maps to NM_080282.3 Y999Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:67197666 T>C maps to NM_080282.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:67150375 C>A maps to NM_080282.3 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:215831647 G>A maps to NM_173076.2 S1936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:215840711 C>T maps to NM_173076.2 L1726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:215851336 G>C maps to NM_173076.2 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr2:215896612 G>A maps to NM_173076.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr2:215855659 G>A maps to NM_173076.2 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:48259100 A>G maps to NM_152701.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:48267013 C>T maps to NM_152701.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:48311893 C>T maps to NM_152701.3 F877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:48559635 G>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:48266876 G>T maps to NM_152701.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:48522714 T>A maps to NM_152701.3 A4379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr7:48319310 C>A maps to NM_152701.3 S2840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr7:48285533 C>A maps to NM_152701.3 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:48313942 T>C maps to NM_152701.3 G1560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr7:48335403 T>G maps to NM_152701.3 T3021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:48684350 G>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:48314309 G>T maps to NM_152701.3 E1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr9:139916868 C>A maps to ENST00000355090 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr9:139909523 T>A maps to ENST00000355090 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr9:139912310 C>T maps to ENST00000355090 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr16:2331209 G>T maps to NM_001089.2 R1393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr16:2347369 C>A maps to NM_001089.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr16:2369698 T>C maps to NM_001089.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:2331438 C>A maps to NM_001089.2 L1369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:2326793 G>A maps to NM_001089.2 L1666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:2349431 C>T maps to NM_001089.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:2373533 G>T maps to NM_001089.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr16:2350062 G>C maps to NM_001089.2 Y518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:94497570 G>A maps to NM_000350.2 V1297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:94502904 C>A maps to NM_000350.2 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:94564445 C>A maps to NM_000350.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:94463497 C>T maps to NM_000350.2 A2216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:94473854 T>C did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:94466450 C>A maps to NM_000350.2 L2140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr17:67282382 C>T maps to ENST00000392677 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr17:67081323 C>G did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:1055128 C>A maps to NM_019112.3 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:1051538 T>C maps to NM_019112.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:1049353 C>T maps to NM_019112.3 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:1049376 C>T maps to NM_019112.3 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:1056366 C>G maps to NM_019112.3 A1485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:1058926 G>A maps to NM_019112.3 R1796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:1056968 G>A maps to NM_019112.3 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr17:66914253 C>A maps to NM_007168.2 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:66881393 G>T maps to NM_007168.2 I1124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:67045445 C>A maps to NM_080283.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:66982357 C>A maps to NM_080283.3 V1385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:67041416 G>C maps to NM_080283.3 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:87174182 C>A maps to NM_000927.3 G674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:87135325 G>A maps to NM_000927.3 Q1175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:87178834 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:229663026 G>A maps to NM_012089.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:229667458 C>T maps to NM_012089.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr2:169780260 G>A maps to NM_003742.2 T1279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr7:87053340 G>A maps to NM_018849.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr7:87049376 C>T maps to NM_018849.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr7:87035606 G>T maps to NM_018849.2 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:87035753 G>C maps to NM_018849.2 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:20698187 G>A maps to NM_001163941.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:20784958 G>A maps to NM_001163941.1 E1109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr7:20682899 C>A maps to NM_001163941.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:20782507 T>A maps to NM_001163941.1 C1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:20683154 C>A maps to NM_001163941.1 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:220077985 G>A maps to NM_005689.2 N594N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:74284973 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:74282202 T>C did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr16:16219668 C>T maps to ENST00000399408 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr16:16108448 C>T maps to ENST00000399408 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr16:16146660 C>T maps to ENST00000399408 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr16:16103673 C>T maps to ENST00000399408 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr6:43410727 C>T maps to NM_033450.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:43414986 G>T maps to NM_033450.2 G1154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:43400086 A>G maps to NM_033450.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:43403604 C>G maps to NM_033450.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:43417158 G>C did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr6:43410820 C>G maps to NM_033450.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:48212567 C>A maps to NM_032583.3 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr16:48256529 T>A maps to NM_032583.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr16:48264454 C>T maps to NM_032583.3 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr16:48209317 G>A maps to NM_032583.3 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr16:48249216 G>A maps to NM_032583.3 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr16:48121986 G>T maps to NM_033226.2 S1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr16:48134805 G>C maps to NM_033226.2 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:101560141 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:183696425 C>T maps to NM_005688.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:183667578 G>A maps to NM_005688.2 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:183669785 G>A maps to NM_005688.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr16:16302586 C>G maps to NM_001171.5 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr16:16278886 G>A maps to NM_001171.5 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:17485035 C>T maps to ENST00000302539 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:17430030 C>A maps to ENST00000302539 E911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:17426063 C>T maps to ENST00000302539 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:17450147 G>T maps to ENST00000302539 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:17464793 G>T maps to ENST00000302539 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:17474671 T>C maps to ENST00000302539 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:17464297 G>C maps to ENST00000302539 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:22047069 C>T maps to NM_005691.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:22046973 G>C maps to NM_005691.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:22068691 A>T maps to NM_005691.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:21998677 G>T maps to NM_005691.2 Y985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:152991558 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:153005582 A>G did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:153001940 G>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:39967557 C>A maps to NM_005164.3 G655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:94930374 C>T maps to ENST00000454898 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr14:74764640 G>A maps to NM_005050.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:150921188 G>A maps to NM_005692.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:150921901 G>A maps to NM_005692.3 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:150916196 G>A maps to NM_005692.3 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr3:183904635 C>T maps to NM_018358.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:183906896 G>A maps to NM_018358.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr3:183907052 C>T maps to NM_018358.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:183907719 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:89052212 C>T maps to NM_004827.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:119031279 C>T maps to NM_001142505.1 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:119025562 T>C maps to NM_001142505.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:119031261 G>A maps to NM_001142505.1 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:119027672 G>A maps to NM_001142505.1 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:119020851 G>A maps to NM_001142505.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:119029032 C>G maps to NM_001142505.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr2:44051082 C>A maps to NM_022436.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:44099382 C>T maps to NM_022437.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:27351983 G>A maps to NM_032604.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:25284236 G>T maps to NM_015600.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr13:108882198 A>C maps to NM_032859.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr14:23072982 G>A maps to NM_022060.2 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:17405195 G>A maps to NM_024527.4 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr19:17411738 C>G maps to NM_024527.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:100570765 G>C maps to ENST00000471714 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:100594367 C>G maps to ENST00000471714 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr3:100472661 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:100471740 G>C maps to ENST00000471714 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:100471738 C>A maps to ENST00000471714 E1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:133760616 C>A maps to NM_007313.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:133760252 C>G maps to NM_007313.2 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr9:133760964 G>A maps to NM_007313.2 E1115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:179087824 G>A maps to NM_007314.3 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr1:179084072 C>A maps to NM_007314.3 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr10:116232759 T>C maps to ENST00000277895 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:116331077 C>A maps to ENST00000277895 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:8108230 G>A maps to NM_001130083.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr4:8046941 G>T maps to NM_001130083.1 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:148577923 C>A maps to NM_014945.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:150558047 G>A maps to ENST00000416793 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:150554700 C>T maps to ENST00000416793 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:150553563 G>T maps to ENST00000416793 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr17:910479 C>A maps to NM_021962.2 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr17:1028613 G>T maps to NM_021962.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr8:107773333 C>G maps to NM_139166.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:107782076 G>A maps to NM_139166.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr3:127396372 C>T maps to NM_172027.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:127399245 C>T maps to NM_172027.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr17:35598927 C>G maps to NM_198834.1 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr17:35487069 G>T maps to NM_198834.1 T1918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr17:35591901 G>A maps to NM_198834.1 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:109644570 G>A maps to NM_001093.3 E990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:109650736 C>T maps to NM_001093.3 Q1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:109665237 G>T maps to NM_001093.3 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr12:109698426 G>T maps to NM_001093.3 P2213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:109702912 A>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:109637323 C>T maps to NM_001093.3 H915H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:112147355 C>T maps to NM_001136538.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:112191649 C>T maps to NM_001136538.1 R995R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:132294744 G>A maps to NM_032169.4 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:132322142 C>A maps to NM_032169.4 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:134130961 C>T maps to NM_014384.2 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:128615307 G>A maps to NM_014049.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:128612405 C>T maps to NM_014049.4 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:128629609 G>T maps to NM_014049.4 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr15:89401962 T>C maps to NM_013227.3 T2049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr15:89401083 C>T maps to NM_013227.3 S1756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr17:7253319 G>C maps to NM_014716.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr3:195027346 T>A did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr3:195027281 G>T maps to NM_012287.5 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:1233770 C>A maps to NM_030649.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:1233243 G>A maps to NM_030649.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:160198421 C>G maps to NM_005891.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr17:32483083 G>A maps to NM_001094.4 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:31438961 C>A maps to NM_183377.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr17:32483482 G>T maps to NM_001094.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:150746349 G>T maps to NM_020321.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:220401787 G>A maps to NM_018674.4 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:44102760 G>C maps to NM_032592.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr11:44072936 C>T maps to NM_001031854.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:44074599 G>C maps to NM_001031854.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr16:67694321 T>A maps to NM_001082486.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr16:67694090 G>A maps to NM_001082486.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr16:67694087 C>T maps to NM_001082486.1 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr17:61560818 A>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:61557860 C>T maps to NM_000789.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:15591559 C>A did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:15609978 C>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:15605981 C>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:100490046 C>G maps to NM_000665.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr14:23549780 T>G maps to NM_014977.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr14:23562721 G>C maps to NM_014977.3 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr14:23549969 C>A maps to NM_014977.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:40030068 C>T maps to ENST00000401700 Q923Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr2:135616875 C>A maps to NM_138326.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr5:80626671 G>A maps to NM_130767.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:74060559 C>T maps to NM_152331.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:74061928 G>A maps to NM_152331.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:6409850 T>A maps to NM_007274.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:6341203 C>T maps to NM_007274.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:23723172 T>C did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr17:73945423 C>A maps to NM_004035.6 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:73945423 C>A maps to NM_004035.6 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:73969780 G>A maps to NM_007292.5 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:58514544 G>A maps to NM_003500.3 N377N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-56-6545-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:111551741 C>G maps to NM_001142807.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:147120110 G>T maps to NM_016361.3 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:147126409 C>A maps to NM_016361.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr1:147131641 C>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:140998307 A>T maps to NM_001037172.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr3:132075646 T>C maps to NM_001134194.1 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr3:132056299 T>C maps to NM_001134194.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:132071601 T>C maps to NM_001134194.1 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr12:6756071 C>T maps to NM_032489.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:70823554 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:70830663 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:70832779 T>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:78471959 C>A maps to NM_015162.4 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:78471989 G>A maps to NM_015162.4 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:78500386 G>A maps to NM_015162.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr15:78474487 C>G did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr15:78473260 C>A maps to NM_015162.4 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:6151738 G>T maps to NM_030924.3 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr17:48551023 A>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:185687113 C>G maps to NM_001995.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:108921306 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:108926549 C>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr10:114187010 C>T maps to NM_016234.3 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:131296314 C>T did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr16:20693759 G>A maps to NM_052956.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr16:20673195 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:20638572 C>T maps to NM_052956.2 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr16:20702438 A>T maps to NM_052956.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr16:20682917 G>A maps to NM_052956.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:20494414 C>T maps to NM_001010845.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr16:20476942 C>T maps to NM_001010845.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr16:20471531 C>A maps to NM_001010845.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr16:20494468 A>G maps to NM_001010845.2 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr16:20494477 C>G maps to NM_001010845.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr16:20471498 C>A maps to NM_001010845.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr16:20480939 A>G maps to NM_001010845.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr16:20477011 T>A maps to NM_001010845.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:20548623 G>A maps to NM_182617.3 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr16:20551989 T>A maps to NM_182617.3 K539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr16:20554479 T>G maps to NM_182617.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr16:20554473 A>G maps to NM_182617.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr16:20548680 C>A maps to NM_182617.3 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:7469834 C>T maps to NM_001080454.1 H241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr12:7477187 C>T maps to NM_001080454.1 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr16:20429496 G>T maps to NM_017888.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr16:20442600 T>A maps to NM_017888.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:20451700 T>A maps to NM_017888.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr16:20441053 T>C maps to NM_017888.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr16:20422838 G>A maps to NM_017888.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr20:25002052 A>G maps to NM_032501.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr20:25011461 G>A maps to NM_032501.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr20:33508828 T>C maps to NM_001076552.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr12:81647377 C>T maps to NM_024560.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:229568342 G>A maps to NM_001100.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:229568575 G>A maps to NM_001100.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:229567638 C>A maps to NM_001100.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:229567524 G>A maps to NM_001100.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:229568799 G>C maps to NM_001100.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:229568327 G>C maps to NM_001100.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:229568793 G>A maps to NM_001100.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:56777565 G>T maps to NM_001017992.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr2:74136210 C>T maps to NM_001615.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr3:179287883 G>T maps to NM_004301.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr3:179292255 G>T did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr7:100246220 C>T maps to NM_016188.4 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr7:100244173 C>A maps to NM_016188.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr9:111617376 G>A maps to NM_006686.3 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr9:111617235 G>A maps to NM_006686.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:18152872 C>G maps to NM_030812.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:18152821 C>A maps to NM_030812.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:8808487 G>A maps to NM_178525.3 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr19:8808793 G>T maps to NM_178525.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:69360385 T>A maps to NM_001130004.1 K281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr1:236898980 C>T maps to NM_001103.2 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:236925900 C>A maps to NM_001103.2 Y889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:236894585 G>T maps to NM_001103.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr1:236889287 T>C maps to NM_001103.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:236920892 G>A maps to NM_001103.2 Q754Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:66330313 A>T maps to NM_001104.1 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr19:39207809 G>T maps to NM_004924.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:58678107 G>T maps to NM_018477.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:58701236 C>T maps to NM_018477.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:98275027 G>C maps to NM_005735.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr2:114688951 A>T maps to NM_005721.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:37383747 C>A maps to NM_024855.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:37384651 C>A maps to NM_024855.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr20:37400215 G>A maps to NM_024855.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:127185841 G>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:127185763 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:127185754 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:2938399 G>A maps to NM_080431.4 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:158622652 A>G maps to NM_001111067.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr2:158406770 G>A maps to NM_145259.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:158406866 C>A maps to NM_145259.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:148653895 C>T maps to NM_001616.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr3:52021588 G>T maps to ENST00000463937 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr3:52019411 G>A maps to ENST00000463937 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr3:52022592 A>T maps to ENST00000463937 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:67413198 G>A maps to NM_080658.1 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:123350818 G>A maps to NM_139243.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr4:123329102 C>T maps to NM_139243.3 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr4:123305121 G>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:123333782 C>G maps to NM_139243.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr4:123350788 T>A maps to NM_139243.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:43641145 G>A maps to ENST00000422466 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr15:43638115 G>T maps to ENST00000422466 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr17:42848950 G>A did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr10:127824199 C>A maps to NM_003474.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr10:127737857 C>T maps to NM_003474.4 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr10:127789651 C>T maps to NM_003474.4 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr10:127708297 G>A maps to NM_003474.4 Q879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr10:127760060 G>A maps to NM_003474.4 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:155029675 C>T maps to NM_207197.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr8:39442155 C>A maps to NM_014237.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr8:39564307 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr8:39537689 C>G maps to NM_014237.2 S589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:39495193 C>A maps to NM_014237.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:39495195 G>A maps to NM_014237.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr8:39525514 A>T did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:39466639 G>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr5:156936310 G>T maps to ENST00000430702 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:156947032 C>T maps to ENST00000430702 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr5:156932792 G>T maps to ENST00000430702 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr8:39602413 T>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr8:39627069 A>G maps to NM_001464.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr8:39644559 G>C maps to NM_001464.3 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr8:39606951 C>T maps to NM_001464.3 K631K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:39606912 G>T maps to NM_001464.3 C644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr8:39613368 T>A maps to NM_001464.3 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr14:70925514 T>A maps to NM_003813.2 C433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr7:87564407 G>T maps to NM_021723.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr7:87792410 A>G maps to NM_021723.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr2:207452056 A>T maps to NM_003812.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:207460863 C>A maps to NM_003812.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:207412164 C>T maps to NM_003812.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:175898682 G>A maps to NM_014269.4 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr4:175899082 C>T maps to NM_014269.4 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr4:175899129 G>A maps to NM_014269.4 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:175897023 C>A maps to NM_014269.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr4:175897227 T>A maps to NM_014269.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr8:39111934 G>T maps to NM_145004.5 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:39018483 G>A maps to NM_145004.5 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr8:39068794 C>A maps to NM_145004.5 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr8:24298629 C>T maps to ENST00000380789 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:24324399 C>T maps to ENST00000380789 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr8:38940182 A>T maps to NM_003816.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr8:38880817 G>C maps to NM_003816.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr21:28213383 C>A maps to NM_006988.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr21:28214678 T>C maps to NM_006988.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr19:8670178 C>A maps to NM_030957.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:8651079 G>A maps to NM_030957.2 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:33649738 G>A maps to NM_030955.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr5:33643488 C>T maps to NM_030955.2 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:33624405 G>A maps to NM_030955.2 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:33649684 G>A maps to NM_030955.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr5:33630994 G>A maps to NM_030955.2 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr5:33616177 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:33637840 C>A maps to NM_030955.2 G577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr5:33588802 C>A maps to NM_030955.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:33684121 C>A maps to NM_030955.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr5:33576386 C>G maps to NM_030955.2 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:136304490 T>A maps to NM_139025.3 Y570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:136305594 C>G maps to NM_139025.3 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr9:136319551 C>A maps to NM_139025.3 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:72503415 C>G maps to NM_139155.2 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:130341140 C>T maps to NM_139055.2 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:5242287 C>T maps to NM_139056.2 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr5:5182170 A>T maps to NM_139056.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr5:5146537 C>G maps to NM_139056.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr5:5146246 T>C maps to NM_139056.2 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr5:5235234 C>T maps to NM_139056.2 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr5:5306798 G>A maps to NM_139056.2 A1123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:5237171 C>A maps to NM_139056.2 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr5:5242296 C>T maps to NM_139056.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:5240016 C>G maps to NM_139056.2 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:5232530 C>T maps to NM_139056.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr5:5186345 G>A maps to NM_139056.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:5186324 T>C maps to NM_139056.2 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr15:100533366 G>A maps to NM_139057.2 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr16:77369732 G>T maps to NM_199355.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr16:77398202 G>C maps to NM_199355.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr5:128864306 T>A maps to NM_133638.3 L416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:128957935 C>T maps to NM_133638.3 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:128844852 T>A maps to NM_133638.3 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:178554975 G>C maps to NM_014244.4 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:178562930 G>C maps to NM_014244.4 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:43847771 A>G maps to ENST00000389420 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr12:43750292 T>C maps to ENST00000389420 R1879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:43944793 G>T maps to ENST00000389420 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr12:43822569 G>T maps to ENST00000389420 A1174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:43847810 A>G maps to ENST00000389420 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr12:43824219 C>A maps to ENST00000389420 E1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:43825196 C>A maps to ENST00000389420 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr4:73186500 G>C maps to NM_014243.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:73434419 A>T maps to NM_014243.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr4:73178142 C>A maps to NM_014243.1 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr4:73154570 G>A maps to NM_014243.1 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:161161862 C>T maps to NM_005099.4 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:161167799 T>C maps to NM_005099.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr21:28305219 G>T maps to NM_007038.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr21:28315774 A>T maps to NM_007038.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr21:28305360 C>T maps to NM_007038.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr21:28296371 C>T maps to NM_007038.3 *931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:64484043 C>T maps to NM_197941.2 W903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr5:64483905 G>T maps to NM_197941.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr15:79064109 G>A maps to ENST00000258883 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr11:130297557 C>T maps to NM_007037.4 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:64627561 C>T maps to NM_182920.1 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:64527225 C>T maps to NM_182920.1 L1756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:64627624 G>A maps to NM_182920.1 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:64619204 T>A maps to NM_182920.1 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr9:18474277 G>T maps to NM_001040272.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr9:18776953 C>T maps to NM_001040272.4 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr9:18574087 A>T maps to NM_001040272.4 K100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr9:18777763 G>T maps to NM_001040272.4 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr15:84553953 G>T maps to NM_207517.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr15:84611785 T>A maps to NM_207517.2 C814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:84592671 A>T maps to NM_207517.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:84558880 G>T maps to NM_207517.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:84611356 G>A maps to NM_207517.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:84611827 G>A maps to NM_207517.2 W828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr15:84373178 C>T maps to NM_207517.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:84373179 G>T maps to NM_207517.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:150526474 C>A maps to ENST00000369039 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:150529461 C>T maps to ENST00000369039 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:943783 G>A maps to NM_006869.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:29281554 C>G maps to ENST00000394782 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:29261291 C>T maps to ENST00000394782 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:154574627 T>A maps to ENST00000292205 K207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:154575069 T>C maps to ENST00000292205 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:154562782 G>C maps to ENST00000292205 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:1405818 C>A maps to NM_018702.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr10:1245947 G>A maps to NM_018702.2 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr10:1405756 C>A maps to NM_018702.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:1405855 C>A maps to NM_018702.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr10:1313258 G>A maps to NM_018702.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr16:75637050 C>A maps to NM_012091.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr16:75646399 T>A maps to NM_012091.3 K262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr6:143755109 T>A maps to NM_182503.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:78399616 C>T maps to NM_020421.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr14:78353519 G>C maps to NM_020421.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr7:140373930 C>A maps to NM_052853.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:140373930 C>A maps to NM_052853.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr7:45697427 C>T maps to NM_021116.2 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr7:45701692 G>T maps to NM_021116.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:167847817 A>T maps to NM_018417.4 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:7804717 C>T maps to NM_020546.2 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:7520855 G>T maps to NM_020546.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:7743795 C>A maps to NM_020546.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr2:25061399 C>A maps to NM_004036.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr2:25095474 C>T maps to NM_004036.3 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr3:123044198 G>T maps to NM_183357.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:123166579 C>A maps to NM_183357.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:123036946 G>A maps to NM_183357.2 D758D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:123049851 A>G maps to NM_183357.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:49166092 G>A maps to NM_015270.3 F924F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr16:50326584 A>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:50347963 C>T maps to NM_001114.3 H949H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr8:131797655 G>C maps to NM_001115.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr8:131916110 C>T maps to NM_001115.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:131859753 C>T maps to NM_001115.2 W806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr8:131793094 G>T maps to NM_001115.2 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr8:132052078 T>C maps to NM_001115.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:131812806 A>T maps to NM_001115.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr8:132051972 G>A maps to NM_001115.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:31132349 G>C did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:31124404 C>G maps to ENST00000409489 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr7:31126092 G>T maps to ENST00000409489 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:70933426 C>A maps to NM_001185054.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:111892124 C>T maps to NM_016824.3 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:100200656 C>T maps to NM_000667.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr4:100231998 T>C maps to NM_000668.4 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:100131364 G>A maps to NM_001102470.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:186572226 C>T maps to NM_004797.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:186572424 G>T maps to NM_004797.3 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:202911227 C>A maps to NM_015999.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:77895041 G>A maps to NM_014913.3 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr22:24837042 C>A maps to NM_000675.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr22:24837045 C>G maps to NM_000675.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:112029245 G>A maps to NM_020683.6 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr3:119306407 G>T maps to NM_001125.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:119301093 C>T maps to NM_001125.2 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr13:114107614 G>A maps to NM_138430.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:36558755 C>T maps to NM_017825.2 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr20:4229245 G>C maps to NM_000678.3 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:115804388 C>A maps to NM_000684.2 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:148206669 C>A maps to NM_000024.5 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr22:26083534 C>T maps to NM_005160.3 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr22:26114279 C>T maps to NM_005160.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr14:105204722 G>T maps to NM_199165.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr14:105209528 G>T did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr15:89172626 G>T maps to NM_022767.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr19:3061228 G>C maps to NM_198969.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:3055670 G>C maps to NM_198969.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr4:7820898 C>T did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr4:7844925 C>A maps to NM_001134647.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr5:148709277 G>C maps to NM_152406.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr4:88035844 C>G maps to NM_001166693.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr4:87967423 G>T maps to NM_001166693.1 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:148037236 G>C did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:148037248 G>C did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:148035200 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:148037465 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:148037577 G>C did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:147743937 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:147967501 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:148037296 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:100623892 C>T maps to NM_001025108.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:100343537 C>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:100170905 C>A maps to NM_001025108.1 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr2:100194832 G>A maps to NM_001025108.1 N983N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:100623799 C>A maps to NM_001025108.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr5:132232282 G>T maps to NM_014423.3 S680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:12358934 G>A maps to NM_006796.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr18:12358704 T>A maps to NM_006796.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:74364929 G>T maps to NM_001133.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:76200743 G>T maps to NM_001145526.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr2:64779426 G>T maps to ENST00000422803 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr4:178358673 C>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr2:236653376 C>T maps to NM_001037131.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:58122158 G>T maps to NM_001122772.1 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:58126640 C>A maps to NM_001122772.1 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr7:150840548 C>A maps to NM_031946.4 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr7:150813908 C>T maps to NM_031946.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:51465351 C>A maps to ENST00000416142 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:100151097 C>G maps to NM_006076.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr5:76331381 G>T maps to NM_018046.4 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:141315302 C>T maps to NM_018238.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:100379263 C>T maps to ENST00000311030 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:32138255 C>T maps to NM_032741.4 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr6:32137187 C>A maps to NM_032741.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr21:45391323 G>A maps to NM_001037553.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:161574441 G>C maps to NM_020133.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr6:161587396 C>T maps to NM_020133.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:161574453 C>A maps to NM_020133.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:161587444 C>A maps to NM_020133.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr4:84519332 G>C did not map to a codon.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr2:178402886 C>T maps to NM_003659.3 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:957792 C>T maps to NM_198576.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:979736 C>T maps to NM_198576.2 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:230846074 C>A maps to NM_000029.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:230838997 A>T maps to NM_000029.3 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:230838937 G>T maps to NM_000029.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:88203361 C>A maps to ENST00000395847 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:115304284 G>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:115304241 C>T did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:115304402 C>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:115304521 G>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:241817437 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:35025918 C>T maps to NM_031900.3 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:35047981 T>A maps to NM_031900.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:247050611 T>C maps to ENST00000428671 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:247040361 G>A maps to ENST00000428671 Q981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:247076561 T>C maps to ENST00000428671 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:110557397 C>T maps to NM_006621.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:27876979 G>C maps to NM_001029882.2 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr1:27878008 G>A maps to NM_001029882.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:27877042 C>G maps to NM_001029882.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:135784437 C>T maps to NM_017651.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:62293704 G>A maps to NM_001620.1 S2728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:62286540 T>C maps to NM_001620.1 E5116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr11:62294835 G>T maps to NM_001620.1 P2351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:62290293 C>T maps to NM_001620.1 E3865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:62293632 T>A maps to NM_001620.1 A2752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr11:62301161 T>A maps to NM_001620.1 K243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr11:62287530 G>C maps to NM_001620.1 P4786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:62287587 A>T maps to NM_001620.1 P4767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:62259291 C>T maps to NM_024060.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:105412214 G>A maps to NM_138420.2 I3191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:105420407 G>A maps to NM_138420.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr14:105405269 G>T maps to NM_138420.2 I5506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr14:105413876 G>C maps to NM_138420.2 A2637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:105418570 C>A maps to NM_138420.2 E1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr14:105409711 C>A maps to NM_138420.2 E4026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr14:105409052 C>G maps to NM_138420.2 L4245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr14:105409190 C>T maps to NM_138420.2 V4199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr14:105406082 G>A maps to NM_138420.2 F5235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr14:105409871 C>T maps to NM_138420.2 K3972K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr14:105409901 C>A maps to NM_138420.2 T3962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:105419198 C>A maps to NM_138420.2 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:105410522 C>A maps to NM_138420.2 A3755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:105409052 C>G maps to NM_138420.2 L4245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:105417071 G>C maps to NM_138420.2 L1572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr14:105415304 C>G maps to NM_138420.2 P2161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr14:105415979 T>C maps to NM_138420.2 K1936K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr14:105412025 G>A maps to NM_138420.2 D3254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr14:105412520 G>A maps to NM_138420.2 D3089D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr14:105411848 G>A maps to NM_138420.2 F3313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:105415985 G>A maps to NM_138420.2 D1934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr14:105423995 C>T maps to NM_138420.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:105420485 G>T maps to NM_138420.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr5:376725 C>A maps to NM_020731.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr5:427953 G>T maps to NM_020731.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:186333535 G>T maps to ENST00000273784 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr12:8758042 G>A maps to NM_020661.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr1:222867550 C>A did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr6:31584146 G>T maps to NM_001623.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:129270689 C>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr22:21331175 G>A maps to NM_144704.2 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:106960404 G>T maps to NM_001624.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr6:106968997 C>G maps to NM_001624.2 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr6:106973216 T>A maps to NM_001624.2 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:159043195 C>A maps to NM_004833.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:159035951 G>A maps to NM_004833.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:159043274 G>T maps to NM_004833.1 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:6329101 C>T maps to NM_014336.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:6328913 C>A maps to NM_014336.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr21:45709878 T>C maps to NM_000383.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr21:45713058 G>T did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:4772100 G>A maps to NM_018836.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr1:4772134 G>T maps to NM_018836.3 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:33480160 C>A maps to NM_001625.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:77752624 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:77759492 C>A maps to NM_174858.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr14:96909081 G>T maps to NM_152327.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:19861528 C>G maps to NM_007202.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr13:42877379 G>T maps to NM_016248.2 E1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:151671464 G>T maps to NM_005100.3 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:151672420 C>T maps to NM_005100.3 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr15:86270385 G>A maps to NM_006738.4 G2308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr15:86124589 A>G maps to NM_006738.4 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr15:86259124 C>T maps to NM_006738.4 S1906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr15:86122468 C>T maps to NM_006738.4 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:119053903 G>C did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr23:119048813 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr9:112898996 G>A maps to NM_007203.4 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr9:112898754 G>T maps to NM_007203.4 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:49957416 G>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:49955709 C>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:49957891 G>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:49957273 A>C did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:49958334 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:49958853 G>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:49958014 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr23:49955643 C>A did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr14:33014469 C>G maps to NM_004274.4 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:33290636 G>A maps to NM_004274.4 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:33292104 G>T maps to NM_004274.4 E1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr14:33014755 C>T maps to NM_004274.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:131481247 G>A maps to ENST00000431975 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr7:91709169 C>T maps to NM_005751.4 Q2575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr7:91631105 G>C maps to NM_005751.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:91699517 A>T maps to NM_005751.4 K2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr7:91714870 T>C maps to NM_005751.4 Y2965Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:91709279 A>G maps to NM_005751.4 L2611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:109954161 T>A maps to NM_001145128.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr6:109867264 C>T maps to NM_001145128.2 Q1010Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:117103886 C>T maps to NM_030767.4 A1331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:109380321 C>A maps to NM_152763.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:109394331 G>A maps to NM_152763.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:46034828 C>A maps to NM_153326.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:46027543 T>C maps to NM_153326.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:134260592 C>T maps to ENST00000418096 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:5040914 C>A maps to NM_001354.4 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr7:137773400 C>A maps to NM_005989.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:40761066 C>T maps to NM_001626.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:40747907 C>A maps to NM_001626.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:74279237 C>T maps to NM_000477.5 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr3:105260526 G>A maps to NM_001627.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr3:105250888 C>A maps to NM_001627.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:105264154 G>A maps to NM_001627.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr3:105250903 A>G maps to NM_001627.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:105250888 C>A maps to NM_001627.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr19:49965238 C>T maps to NM_153329.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:49962965 G>A maps to NM_153329.3 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr9:75526975 G>T maps to NM_000689.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr15:101436238 C>T maps to NM_000693.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:125877438 G>A maps to ENST00000273450 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:125822660 C>A maps to ENST00000273450 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:125822660 C>A maps to ENST00000273450 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr12:105445869 A>G maps to NM_001034173.3 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr17:19646724 C>A maps to NM_000691.4 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:67782874 C>T maps to NM_001161473.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:67789266 G>A maps to NM_001161473.1 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:67786654 G>A maps to NM_001161473.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:19212113 G>C maps to NM_003748.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:24505194 C>T maps to NM_170740.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:24523059 C>T maps to NM_170740.1 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr14:74539004 A>T maps to NM_005589.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:125894940 C>T maps to NM_001182.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:125930764 C>T maps to NM_001182.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:165636577 G>T maps to NM_000696.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr16:30080175 G>A maps to ENST00000395248 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:26902292 G>A maps to NM_005165.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr12:34175629 A>T maps to NM_032834.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:38714684 A>G maps to NM_001013620.3 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr22:50307062 C>A maps to NM_024105.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr23:110970886 G>T did not map to a codon.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr23:110928308 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:110951367 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:111002982 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:110979953 A>G did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:111003209 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:95448642 G>T maps to NM_144988.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr3:125651528 C>A maps to NM_001195223.1 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:101980728 G>A maps to NM_033087.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:101980674 C>G maps to NM_033087.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr3:183963050 C>T maps to NM_005787.5 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:183960602 G>C maps to NM_005787.5 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr13:37573413 C>T maps to NM_013338.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr11:111706941 G>T maps to ENST00000428306 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:29754881 C>A maps to NM_004304.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr2:29917800 G>A maps to NM_004304.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr11:43923169 G>A maps to NM_139178.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:43923275 G>T did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr7:102098134 C>T maps to NM_017621.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr7:102098422 A>G maps to NM_017621.3 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr19:6374903 C>A maps to NM_032306.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:107424702 C>G maps to ENST00000417449 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:3744988 C>T maps to ENST00000403787 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:3730596 C>A maps to ENST00000403787 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:3727498 C>A maps to ENST00000403787 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr2:73677451 A>T maps to NM_015120.4 S1265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:73716777 G>T maps to NM_015120.4 R2563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:73717529 C>G maps to NM_015120.4 S2814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr2:73826589 A>C maps to NM_015120.4 S3869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:73678880 C>T maps to NM_015120.4 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:73717020 C>A maps to NM_015120.4 S2644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:73762075 G>T maps to NM_015120.4 G3302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:73717647 A>G maps to NM_015120.4 L2853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:73675342 G>A maps to NM_015120.4 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr17:7979000 C>A maps to NM_001139.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr17:7950906 G>T maps to NM_001141.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr10:45878094 C>A maps to NM_000698.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:233322010 C>A maps to NM_001631.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:233323622 G>T maps to NM_001631.3 G452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:113353609 C>T maps to NM_025144.3 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr4:113351677 G>A maps to NM_025144.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr18:56202300 C>G maps to NM_052947.3 T1706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr18:56246129 G>A maps to NM_052947.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr18:56149152 T>A maps to NM_052947.3 K2139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr18:56202163 G>C maps to NM_052947.3 S1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr18:56205343 G>C maps to NM_052947.3 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:85360217 G>C maps to NM_020778.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr15:85407729 G>A maps to NM_020778.4 L1721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr15:85400800 G>T maps to NM_020778.4 G1146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:21887194 C>T maps to NM_000478.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:233246045 C>A maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:233272585 G>A maps to NM_031313.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:202625740 C>A maps to NM_020919.3 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:202593786 G>T maps to NM_020919.3 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:202582798 C>A did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr2:202590177 C>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:202632081 C>T maps to NM_020919.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr3:46728559 C>A maps to NM_147129.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:202430540 C>G maps to NM_001168221.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr2:202501503 G>A maps to ENST00000409099 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:85674242 C>A maps to NM_006982.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:44289132 C>A maps to NM_021926.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr11:44286712 G>T maps to NM_021926.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr11:44286613 C>G maps to NM_021926.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:33521008 G>A maps to NM_152462.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:33520840 C>A maps to NM_152462.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:33520777 C>A maps to NM_152462.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr17:33520468 T>C maps to NM_152462.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:33520924 G>A maps to NM_152462.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr17:33520726 G>T maps to NM_152462.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr17:33520408 T>A maps to NM_152462.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr17:7386196 T>C maps to NM_001102614.1 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:34004780 C>A maps to NM_001167595.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr4:71472445 G>C maps to NM_016519.4 *448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:111214268 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-22-5472-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:11316884 C>T did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr23:11316381 G>C did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:11316789 A>G did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr24:6738082 A>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr24:6736491 A>G did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr12:53819612 C>T maps to NM_020547.2 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr12:53823385 C>T maps to NM_020547.2 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:53818147 G>A maps to NM_020547.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr11:118074379 C>A maps to NM_001098526.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:109444272 C>T did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:112058617 C>A did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:112021835 C>A did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:112033994 G>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:112022908 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:94563320 G>T maps to NM_130847.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:134084661 G>A maps to ENST00000514516 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr1:115222974 G>T maps to NM_000036.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr11:10483249 G>T maps to NM_000480.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr11:10503749 A>G maps to NM_000480.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:38431390 T>A maps to NM_001635.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:38424478 G>T maps to NM_001635.3 Y676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr7:38433814 C>G did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr7:38471794 T>C maps to NM_001635.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:38502669 C>A maps to NM_001635.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr1:104114877 G>T maps to ENST00000305865 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr1:104120395 T>A maps to NM_020978.3 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:66251839 G>T did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:112539963 A>T maps to NM_022662.2 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:112608442 C>A maps to NM_022662.2 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:112536326 G>C maps to NM_022662.2 L1770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr2:112550113 C>A maps to NM_022662.2 E1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr9:140076196 C>T maps to NM_013366.3 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr4:25391797 G>T maps to ENST00000510092 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:121789998 C>A maps to NM_016237.4 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:110834112 C>A maps to NM_016238.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr14:77272758 C>T maps to NM_015305.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:213173693 T>C maps to NM_144567.3 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr1:213186486 G>A maps to NM_144567.3 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:108348442 G>A maps to NM_001146.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:108264187 C>A maps to NM_001146.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr8:108334130 T>C maps to NM_001146.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:6378764 G>A maps to NM_001147.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr20:853650 G>A maps to NM_015985.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr20:865719 C>A did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:178834179 A>T maps to NM_004673.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:63066782 G>T maps to NM_014495.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:101762073 G>T maps to NM_178127.4 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:101771161 T>C maps to NM_178127.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr19:10203303 G>C maps to NM_031917.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr8:41547780 G>T maps to ENST00000415018 L1356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr8:41530290 G>C maps to ENST00000415018 T1559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr8:41574570 T>C did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:41615562 G>T maps to ENST00000415018 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr8:41615631 C>G maps to ENST00000415018 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:41519459 C>G did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr8:41554237 C>T maps to ENST00000415018 E897E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:41753902 C>G maps to NM_001142446.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:114257062 C>T maps to NM_001148.4 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:114257119 A>T maps to NM_001148.4 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr4:114120240 A>T maps to NM_001148.4 G120G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-22-1016-01A-01D-1521-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr4:114267165 G>C maps to NM_001148.4 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr4:114279463 G>C maps to NM_001148.4 T3230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr4:114278131 T>A maps to NM_001148.4 A2786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:114276262 G>A maps to NM_001148.4 Q2163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr4:114277102 A>G maps to NM_001148.4 L2443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr4:114163340 C>A maps to NM_001148.4 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:114251537 A>T maps to NM_001148.4 R1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr10:61832076 T>C maps to NM_020987.2 T2854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr10:61830137 G>A maps to NM_020987.2 Q3501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:61834413 C>T maps to NM_020987.2 Q2075Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr10:61835766 G>T maps to NM_020987.2 T1624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:61835775 G>A maps to NM_020987.2 S1621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:190569857 G>A maps to NM_144708.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr15:65219161 C>A maps to NM_182703.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:54534321 G>A did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr17:54428147 G>C maps to NM_153228.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:54428249 G>A maps to NM_153228.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:14711349 C>A maps to NM_054027.4 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr5:14758687 G>C maps to NM_054027.4 Y111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:14871535 G>C maps to NM_054027.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:92027142 C>T maps to NM_019004.1 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr7:92027578 A>G maps to NM_019004.1 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr7:91974290 G>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr7:92027803 G>A maps to NM_019004.1 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:92019372 A>T maps to NM_019004.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:113266891 C>T maps to NM_178510.1 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:113265685 G>A maps to NM_178510.1 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:17396326 C>A maps to NM_152363.4 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:133304629 G>T maps to NM_015114.1 S868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr12:133306453 G>C maps to NM_015114.1 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:241465143 G>A maps to ENST00000401804 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr2:241468503 G>A maps to ENST00000401804 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:241468617 C>A maps to ENST00000401804 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:72850213 C>T did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr10:92675930 A>G maps to NM_014391.2 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr16:89350993 C>T maps to NM_013275.4 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr16:89351185 C>T maps to NM_013275.4 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr16:89348929 G>C maps to NM_013275.4 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr16:89352525 C>T maps to NM_013275.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:89348548 C>T maps to NM_013275.4 E1467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr18:9254527 C>G maps to NM_015208.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:9263832 C>T maps to NM_015208.3 R1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:110450961 G>T maps to NM_033121.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr17:27935920 C>T maps to NM_152345.4 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr17:27936293 G>T did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr4:74021825 G>T maps to NM_032217.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr4:73986009 C>G maps to NM_032217.3 A1298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr4:73941986 T>C maps to NM_032217.3 A2591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr4:74005578 T>G maps to NM_032217.3 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:73987359 T>G maps to NM_032217.3 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr4:73986693 A>G maps to NM_032217.3 N1251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:67951984 A>G maps to NM_001012419.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:97505484 G>A maps to NM_144994.7 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:4217103 A>G maps to ENST00000262970 E739E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr10:27324213 T>C maps to NM_014915.2 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:27368048 G>T maps to NM_014915.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr10:27366455 A>G maps to NM_014915.2 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:27306603 C>A maps to NM_014915.2 E1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr19:33132954 G>C maps to NM_032139.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr19:33113387 C>T maps to NM_032139.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:33117719 G>C maps to NM_032139.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:33135332 C>A maps to NM_032139.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr3:15762484 T>C maps to NM_015199.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:37418827 C>T maps to ENST00000374660 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:37442555 A>G maps to ENST00000374660 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr10:37421199 G>C maps to ENST00000374660 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr10:37421232 G>A maps to ENST00000374660 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr10:37508495 A>T maps to ENST00000374660 R1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr10:37438703 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr10:37422843 C>A maps to ENST00000374660 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr10:37508512 A>C maps to ENST00000374660 T1354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr10:37430820 G>A maps to ENST00000374660 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:37508126 C>T maps to ENST00000374660 Q1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:37430679 A>G maps to ENST00000374660 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:37506637 A>G maps to ENST00000374660 Q1096Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:37454037 A>C maps to ENST00000374660 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:145473834 G>A maps to NM_001039888.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr5:79854373 T>A maps to NM_001004441.2 K489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:145566771 G>T maps to NM_144698.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:98177126 C>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:197870508 C>T maps to NM_001195144.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:197878391 C>G maps to NM_001195144.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr8:101540108 G>T maps to NM_198401.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:94231406 G>C maps to NM_017704.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:94231410 C>T maps to NM_017704.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr20:10036304 C>G maps to NM_198798.1 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr20:10032358 T>C maps to NM_198798.1 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr4:125599885 T>C maps to NM_020337.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr4:125599866 G>A maps to NM_020337.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr4:125590640 G>C maps to NM_020337.2 S1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:56645803 G>A maps to NM_173595.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:55396066 G>A maps to NM_024669.2 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:118893502 G>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr6:90323536 T>A maps to ENST00000339746 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:90333769 G>A maps to ENST00000339746 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr7:117874895 G>T maps to ENST00000357099 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:34957032 G>T maps to NM_015245.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:35027961 G>T maps to NM_015245.2 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:34985289 G>T maps to NM_015245.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:34937796 G>T maps to NM_015245.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr12:99478770 A>G maps to NM_152788.3 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:99793514 G>T maps to NM_152788.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr12:99145240 T>A maps to NM_152788.3 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr16:4747367 G>A maps to NM_133450.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr16:21262053 G>A maps to NM_145865.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:70033893 C>T maps to NM_018043.5 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:70009403 G>A maps to NM_018043.5 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr3:43621947 C>T maps to NM_018075.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:43640089 T>A maps to NM_018075.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:5687655 G>A maps to ENST00000356134 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr12:5853392 C>G maps to ENST00000356134 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr12:5687598 C>T maps to ENST00000356134 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr12:5722117 C>A maps to ENST00000356134 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:26621131 G>T maps to NM_031418.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:26465321 G>A maps to NM_031418.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:26663520 T>C maps to NM_031418.2 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:26663548 G>T maps to NM_031418.2 G750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:26620409 A>T maps to NM_031418.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:26677982 C>A maps to NM_031418.2 Y906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr12:101514369 A>G maps to ENST00000392977 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:101488069 G>T maps to ENST00000392977 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:101336159 G>A maps to ENST00000392977 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:22294420 G>T maps to NM_213599.2 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr11:22261200 C>T maps to NM_213599.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:22225350 G>T maps to NM_213599.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:22242674 C>A maps to NM_213599.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:22249066 C>A maps to NM_213599.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:45771834 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:45744460 C>G maps to NM_001142679.1 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:242142806 C>T maps to NM_001001891.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:242128058 C>G maps to NM_001001891.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr19:17435527 G>T maps to NM_020959.2 S1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr19:17438617 G>T maps to NM_020959.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr11:418530 G>T maps to NM_001012302.2 S730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:428391 G>A maps to NM_001012302.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:100756943 C>G maps to NM_006401.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr4:165118455 C>A maps to NM_012403.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr15:90347585 C>T maps to NM_001150.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr4:80990633 C>T maps to NM_001145794.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:46147482 T>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:75782447 G>T maps to NM_000700.1 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr10:81917737 G>T maps to NM_145869.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr4:79525537 A>G maps to NM_005139.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr2:70052637 A>T maps to NM_001153.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr4:122592700 C>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr5:150518925 G>C maps to NM_001155.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:150496741 C>A did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:150502572 C>T did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr5:150505988 C>A maps to NM_001155.4 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:75157984 G>A maps to NM_004034.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:150958866 G>A maps to NM_003568.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr7:36698785 G>C maps to NM_001177506.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:36633999 C>A maps to NM_001177506.1 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr17:40997602 A>G maps to NM_009590.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:40996817 C>T maps to NM_009590.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr17:41007478 C>A maps to NM_003734.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:41004562 G>T maps to NM_003734.2 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr4:113189327 A>G maps to NM_018569.4 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr22:29727775 C>T maps to NM_001127.3 Q813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr22:29745308 C>A maps to NM_001127.3 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr22:29726513 C>T maps to NM_001127.3 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:29754885 G>A maps to NM_001127.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr16:71803594 G>C maps to ENST00000423132 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr19:16317170 G>A maps to NM_001130524.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr7:100799994 C>T maps to NM_001283.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr17:34009758 G>A maps to NM_001030006.1 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:183899528 T>C maps to ENST00000411763 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:77334915 C>T maps to NM_003664.3 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:77423969 G>A maps to NM_003664.3 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr15:83349907 G>A maps to NM_004644.3 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr15:83331596 G>T maps to NM_004644.3 Y875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:2102252 G>A maps to ENST00000355272 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:2121813 G>A maps to ENST00000355272 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr8:42023009 G>A maps to NM_006803.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr15:90378851 C>A maps to ENST00000398333 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:90378815 T>C maps to ENST00000398333 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:114445387 C>A maps to NM_006594.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr15:51242118 G>C maps to NM_007347.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr7:99699369 G>A maps to ENST00000429084 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:99076988 C>T maps to NM_181861.1 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:29346758 G>A maps to NM_005503.3 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr15:29346392 C>T maps to NM_005503.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr15:29393968 T>C maps to NM_005503.3 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:29367138 G>T maps to NM_005503.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr15:29390703 G>T maps to NM_005503.3 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr15:29346290 C>T maps to NM_005503.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr11:6423355 G>C maps to ENST00000389906 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:26800680 C>T maps to NM_019043.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:26830588 A>T maps to NM_019043.3 K375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr10:26830516 C>A maps to NM_019043.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:40832491 C>T maps to NM_004307.1 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr4:41016209 G>A maps to NM_004307.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:41016137 C>A maps to NM_004307.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr5:112154687 C>G maps to NM_001127510.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr5:112174551 C>T maps to NM_001127510.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr5:112174042 G>T maps to NM_001127510.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:1468498 C>G maps to NM_005883.2 P1733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr18:10485544 G>C maps to ENST00000423585 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr18:10487806 C>T maps to ENST00000423585 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:57035881 G>T maps to NM_153360.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr3:49713630 G>A maps to ENST00000438011 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:55028745 C>A did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:55033378 G>C did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:150239861 G>A maps to NM_001077628.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:43344984 A>T maps to NM_001142930.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr11:43350425 C>G maps to NM_001142930.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:43348095 G>T maps to NM_001142930.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr2:68765101 T>C maps to NM_173545.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:57003958 C>A maps to NM_005161.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr11:57004426 C>A maps to NM_005161.4 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:36367438 G>T maps to NM_001024807.1 V455V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3410-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:161192259 C>A maps to NM_001643.1 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:116691972 C>G maps to NM_000482.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:116661353 G>A maps to NM_052968.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:116661392 G>T maps to NM_052968.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:21228606 G>C maps to NM_000384.2 T3711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:21225417 G>A maps to NM_000384.2 T4292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:21232202 G>A maps to NM_000384.2 R2513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:21232523 C>A maps to NM_000384.2 E2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:21227275 G>A maps to NM_000384.2 T3984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:21229832 C>A maps to NM_000384.2 E3303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:21230880 G>A maps to NM_000384.2 P2953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:21231882 G>A maps to NM_000384.2 V2619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:21242602 C>T maps to NM_000384.2 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:21224841 C>T maps to NM_000384.2 T4484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:21236164 A>G maps to NM_000384.2 N1361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:21229323 G>T maps to NM_000384.2 T3472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:21233859 G>T maps to NM_000384.2 I1960I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:21256231 G>A maps to NM_000384.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr2:21232181 G>A maps to NM_000384.2 R2520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:21252820 C>T maps to NM_000384.2 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr2:21228897 A>C maps to NM_000384.2 P3614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr2:21236224 G>T maps to NM_000384.2 T1341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr2:21232598 G>A maps to NM_000384.2 L2381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:21231682 C>T maps to NM_000384.2 W2686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:21247879 G>A maps to NM_000384.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr2:21237992 G>A maps to NM_000384.2 V1216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr12:7803648 C>T maps to NM_001644.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:41029511 G>T maps to NM_006789.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr22:39357612 C>T maps to NM_001193289.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:45422441 A>T maps to NM_001645.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:116701609 C>T maps to ENST00000360377 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:195295818 G>T maps to ENST00000421243 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:64210727 G>A maps to NM_000042.2 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:64210706 A>T maps to NM_000042.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:64210607 A>T maps to NM_000042.2 C315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:36124923 C>T maps to NM_030642.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr22:36124887 A>T maps to NM_030642.1 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:36055366 C>G maps to NM_030641.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:31624394 C>A maps to NM_019101.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:23886726 C>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:23886747 A>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:23858458 C>A did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:84310881 G>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:84310875 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:84306417 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr21:27372438 G>C maps to NM_000484.3 Y308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:58538058 G>A maps to NM_006380.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:154295501 G>T maps to NM_080429.2 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:50357894 C>A maps to NM_001651.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:50368168 G>A maps to NM_001652.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:50369452 G>C maps to NM_001652.3 *283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:50367132 C>T maps to NM_001652.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr9:33385651 G>A maps to NM_001170.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr16:25238397 G>T maps to NM_001169.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr16:25228739 C>A maps to NM_001169.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:58467216 G>A maps to NM_020980.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:35149100 G>A maps to NM_014691.2 A1450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:35202473 G>A maps to NM_014691.2 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr15:35198839 C>A maps to NM_014691.2 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr23:66766595 G>C did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:66765157 T>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:66766198 C>T did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:66863173 G>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:66943545 C>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:66765850 C>A did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:66931319 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:66766092 C>G did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:47426042 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:47426293 G>C did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:72424247 C>A maps to NM_001040118.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr4:36075361 C>G maps to NM_015230.2 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:36179598 T>C maps to NM_015230.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr4:36135011 C>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:36093523 G>A maps to NM_015230.2 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:36214040 T>G maps to NM_015230.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:141052627 G>A maps to NM_022481.5 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr11:118451965 G>T maps to ENST00000359415 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:228285620 G>A maps to NM_001024228.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:228285653 C>T maps to NM_001024228.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:228285671 A>G maps to NM_001024228.1 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:127230148 C>T maps to NM_001662.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr7:127231093 G>T maps to NM_001662.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr20:61907486 G>A maps to NM_175609.1 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr8:68179409 G>T maps to NM_006421.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr20:47587749 C>T maps to NM_006420.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr4:153784804 A>G maps to NM_001025595.1 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr11:6499299 G>T maps to NM_012402.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:131904927 G>A maps to ENST00000356962 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:121305098 C>A maps to NM_001012659.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:46717597 C>G maps to NM_004308.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr4:148876464 A>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:32926223 G>T maps to NM_014783.3 G442G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-66-2788-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:30919107 C>T maps to NM_001039841.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr10:32106815 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:144381753 C>A maps to NM_018460.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:143913211 G>A maps to NM_018460.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr6:129932708 A>C maps to NM_033515.2 L364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:110450852 G>A maps to NM_020809.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr11:110486302 C>T maps to NM_020809.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:24886904 G>A maps to NM_020824.3 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:49791060 G>C maps to ENST00000417912 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:86896081 G>T maps to NM_001025616.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:69049821 C>T maps to NM_001007231.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:94685904 G>T maps to NM_004815.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:161039354 G>A maps to NM_001025598.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:119134027 C>T maps to NM_020754.2 H1084H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr3:119120969 G>C maps to NM_020754.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr3:119121047 G>A maps to NM_020754.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:119121086 C>T maps to NM_020754.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr11:128844844 C>G maps to NM_001142685.1 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:36273343 G>T maps to ENST00000007510 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:36277799 C>T maps to ENST00000007510 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:130220568 T>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:130218914 G>T did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:130215673 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:130218251 C>G did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:130220304 G>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:130217852 G>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:130218635 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:130218281 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:130217168 A>G did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:130215796 A>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:130217733 A>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:153173228 G>C did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:153173336 G>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr14:32624152 G>A maps to NM_001030055.1 *1503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:11162210 C>A did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:11204421 G>C did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:11682534 G>A did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr23:11204357 T>C did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:11682384 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:57866395 C>A maps to ENST00000393797 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr12:57872973 G>A maps to ENST00000393797 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:15095464 C>T maps to NM_001175.4 W199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr19:42399545 A>T maps to NM_199002.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:42396399 A>C did not map to a codon.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr8:1846691 G>C did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr8:1808300 C>T maps to ENST00000398564 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:17961048 C>A maps to NM_018125.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:17964464 G>T maps to NM_018125.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:17991035 G>A maps to NM_018125.3 W985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:17953965 A>T maps to NM_018125.3 K518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:17948357 G>T did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:156947995 C>T maps to NM_198236.1 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:156917606 C>A maps to NM_198236.1 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:156928543 C>A maps to NM_198236.1 G498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:120352170 G>A maps to NM_015313.2 W1480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr11:120345303 A>G maps to NM_015313.2 E1023E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:8221892 C>A maps to NM_173728.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:3389704 C>T maps to NM_014448.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:3390010 G>T maps to NM_014448.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:73066919 G>A maps to NM_014786.3 E1195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr11:73021926 A>G maps to NM_014786.3 E748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:155921324 C>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:155921324 C>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:155931628 C>A maps to NM_001162383.1 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:56779334 G>T maps to NM_001128615.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr3:56763414 T>C maps to NM_001128615.1 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr4:106510543 T>C maps to ENST00000420470 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr4:106534584 C>G maps to ENST00000420470 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:131801049 C>G maps to NM_015320.2 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:135795453 G>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:135758807 C>T did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:135825760 C>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr13:111932895 G>T maps to NM_001113511.1 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:62974187 G>T did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:62917182 C>T did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:62917067 C>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:62857962 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:62944453 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:62885772 C>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:62885837 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:27100301 C>T maps to NM_006015.4 S1338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:27057764 C>A maps to NM_006015.4 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr1:27105920 G>A maps to NM_006015.4 W1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:27100388 G>A maps to NM_006015.4 Q1367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:157528346 G>T maps to ENST00000367148 T2064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr6:157521978 G>A maps to ENST00000367148 R1457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:157527306 G>T maps to ENST00000367148 G1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:157522134 T>C maps to ENST00000367148 N1509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:46211526 C>T maps to NM_152641.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:46244155 G>T maps to NM_152641.2 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:46233247 C>T maps to NM_152641.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:46240700 G>T maps to NM_152641.2 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr12:46245334 G>A maps to NM_152641.2 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr14:58817844 G>T maps to NM_002892.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr14:58814582 T>G maps to NM_002892.3 L464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:235331885 G>C maps to NM_016374.5 S1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:235383151 G>A maps to NM_016374.5 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:97216903 G>A maps to NM_212481.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr2:97217929 C>T maps to NM_212481.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:97217380 G>A maps to NM_212481.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr10:63816877 G>A maps to NM_032199.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr12:101794927 G>C maps to NM_001177.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:100242387 T>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:100242484 C>T did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr3:160395629 C>T maps to NM_025047.2 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr3:160395289 C>T maps to NM_025047.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr3:160395682 A>G maps to NM_025047.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr16:57282554 C>A maps to NM_012106.3 Y69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr10:104445665 G>A maps to NM_004311.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:12728312 C>G maps to NM_005738.4 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:97510648 G>T maps to NM_177976.1 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr2:153575167 G>A maps to NM_152522.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr6:109175565 A>G maps to NM_032131.4 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr10:23319668 G>T maps to NM_173081.3 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:23248442 G>A maps to NM_173081.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:28233360 C>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:28233219 A>G maps to NM_018076.2 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:28228918 T>A maps to NM_018076.2 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:100809044 A>G did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:100808630 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:100911282 G>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:100912229 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:100911580 G>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr23:100911753 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:100911568 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:100912249 T>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:100880052 T>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:100880488 A>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:101857703 A>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:101857623 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:101857186 G>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:100871325 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:150790442 G>A maps to NM_001668.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr15:80762559 G>T maps to NM_014862.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr12:27553683 A>G maps to NM_020183.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:27540213 C>T maps to NM_020183.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:27573380 C>G maps to NM_020183.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr7:98955992 G>T maps to NM_006409.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:169485280 C>T maps to NM_032487.4 W353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:169485439 G>C maps to NM_032487.4 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr3:169485534 G>T maps to NM_032487.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:35763326 G>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:35778737 C>T maps to ENST00000458225 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:35770810 C>T maps to ENST00000458225 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:69495997 T>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:69498433 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:18121060 C>T maps to NM_015683.1 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:18121408 C>T maps to NM_015683.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr19:18119343 C>T maps to NM_015683.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr15:98509238 T>C maps to NM_183376.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:98511307 C>A maps to NM_183376.2 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr19:4891522 G>T maps to NM_001080523.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr5:78181605 G>A maps to NM_000046.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:2828759 C>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:2864050 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:2867671 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:3021843 C>T did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:3030248 G>C did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:3002639 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:3021943 G>A did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr17:66364802 C>T maps to NM_014960.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:2951309 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:2933301 G>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:2945445 G>A did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:2947376 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:149676782 C>T maps to NM_001012301.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:3680844 C>G maps to NM_004314.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:231131695 A>G maps to NM_022786.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr8:131136347 C>A maps to NM_018482.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr8:131130757 C>A maps to NM_018482.2 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:9528580 C>T maps to NM_003887.2 Y763Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr2:9508555 C>A maps to NM_003887.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr2:9490935 G>A did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:150873366 G>A maps to ENST00000422024 Y457Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:150883937 G>T maps to ENST00000422024 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:15333584 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:15311359 A>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:15311320 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:63444241 C>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:63444977 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:63445175 G>T did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:63445289 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:63445503 C>G did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:5682752 C>T maps to NM_024701.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr7:123256316 C>A maps to NM_080928.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr1:76387992 G>T maps to NM_080868.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:53897776 G>A maps to NM_001164165.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:95166989 C>A maps to NM_016116.2 C400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr15:101169982 C>T maps to NM_198243.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:15268611 G>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:15270381 T>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:15268560 G>C did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr22:30189467 C>T maps to NM_032204.3 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr22:30198080 G>A maps to NM_032204.3 C490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr6:101095149 T>A maps to NM_006828.2 K1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:101296200 G>A maps to NM_006828.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:101076978 C>T maps to NM_006828.2 E1429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr11:8959438 G>T maps to NM_020646.1 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:108169132 C>A maps to NM_203436.2 C47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:108169385 C>T maps to NM_203436.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:14236969 G>A maps to NM_018154.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr17:7011805 C>A maps to NM_080912.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:155449537 C>T maps to ENST00000368346 K1041K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:155348295 G>C maps to ENST00000368346 S2079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:155449246 T>C maps to ENST00000368346 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:65554682 G>T did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:1743267 G>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:1742165 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:1531734 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:1536905 T>C did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr23:1546947 G>C did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:1522274 G>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:1554620 C>T did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr2:190530929 A>G maps to NM_019048.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:190532307 C>T maps to NM_019048.2 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr2:190535245 C>T maps to NM_019048.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:3392562 G>C maps to NM_000049.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr14:104559905 C>T maps to NM_001080464.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:62430620 G>A maps to NM_004318.3 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:62556542 G>A maps to NM_004318.3 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr8:62430121 C>T maps to NM_004318.3 K697K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr16:29917136 C>A maps to NM_181718.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:197072611 T>C maps to NM_018136.4 A1923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:197072092 T>A maps to NM_018136.4 T2096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:197112697 G>A maps to NM_018136.4 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr1:197069638 G>A maps to NM_018136.4 I2914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:197086918 C>T maps to NM_018136.4 Q1355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr1:197073676 T>A maps to NM_018136.4 S1568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:95219629 A>G maps to NM_017680.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:70187819 G>C maps to NM_152792.2 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr17:79974978 G>A maps to ENST00000306729 L640L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-66-2785-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:176992576 G>A maps to ENST00000281881 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:177030383 C>A maps to ENST00000281881 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:176915117 A>T maps to ENST00000281881 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:177001748 T>G maps to ENST00000281881 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:176857302 G>T maps to ENST00000281881 S1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:176903471 G>A maps to ENST00000281881 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:176838112 C>A maps to ENST00000281881 E1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:176915086 C>A maps to ENST00000281881 G750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:177001634 G>T maps to ENST00000281881 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:176915138 G>C maps to ENST00000281881 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:176838083 C>A maps to ENST00000281881 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:176992584 G>T maps to ENST00000281881 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:119202970 C>T maps to ENST00000313400 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr9:119976960 G>A maps to ENST00000313400 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr9:119976865 G>C maps to ENST00000313400 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:31019262 C>T maps to ENST00000375687 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:31022585 C>T maps to ENST00000375687 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:31023202 G>A maps to ENST00000375687 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr20:31017234 G>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr20:31022549 G>T maps to ENST00000375687 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr20:31022722 A>T maps to ENST00000375687 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr18:31324141 C>A maps to NM_030632.1 R1444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr18:31324465 T>C maps to NM_030632.1 L1552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr18:31320004 A>C maps to NM_030632.1 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr18:31326457 C>A maps to NM_030632.1 R2216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr18:31324434 T>C maps to NM_030632.1 A1541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr18:31226213 G>A maps to NM_030632.1 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:31323249 T>C maps to NM_030632.1 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr18:31323870 C>T maps to NM_030632.1 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr18:31325403 C>A maps to NM_030632.1 G1864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:117003718 C>T maps to NM_130768.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr7:117007444 C>T maps to NM_130768.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:124408547 G>T maps to NM_014109.3 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr8:124349884 T>A maps to NM_014109.3 K1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:29195407 A>C maps to NM_024857.3 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr17:29162428 A>T maps to NM_024857.3 K444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:29185177 G>T did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr17:29192759 C>T maps to NM_024857.3 Q1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr17:29192765 C>T maps to NM_024857.3 Q1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr17:29192773 C>T maps to NM_024857.3 A1063A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:3905453 C>T maps to NM_033064.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:123600613 G>A maps to NM_001001976.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:212788545 G>A maps to NM_001674.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr22:39917931 C>G maps to NM_182810.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:161833056 C>T maps to NM_007348.2 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:32088563 G>T maps to NM_004381.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr6:32085723 C>A maps to NM_004381.4 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:14634063 C>A maps to NM_018179.3 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:14577230 G>T maps to NM_018179.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:234178665 G>T maps to ENST00000392018 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:234198997 C>A maps to ENST00000392018 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr11:72536435 C>G maps to NM_033388.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:64681894 G>A maps to ENST00000421419 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:64664300 C>A maps to ENST00000421419 E1733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:96769592 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:96807900 C>T maps to NM_018036.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:107380350 C>T did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr3:11468388 C>T maps to NM_006395.2 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:11350507 C>G maps to NM_006395.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:11383695 C>G maps to NM_006395.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:11389434 G>T maps to NM_006395.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:220089410 G>A maps to NM_024085.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:293669 G>A maps to ENST00000409479 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:292013 A>G maps to ENST00000409479 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:216190788 G>C maps to NM_004044.6 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:108098501 G>A did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr16:81078460 G>A maps to NM_015251.2 Q786Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:81078196 G>A maps to NM_015251.2 E698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:7046109 A>G maps to NM_001940.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr12:7050103 C>T maps to NM_001940.3 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:25925105 G>A maps to NM_024490.3 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:25972343 C>T maps to NM_024490.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr15:25959127 C>A maps to NM_024490.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr15:26026275 G>A maps to NM_024490.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr15:25966981 G>A maps to NM_024490.3 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr15:25924793 T>A maps to NM_024490.3 P1398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr15:25932882 G>T maps to NM_024490.3 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:25925401 C>A maps to NM_024490.3 V1244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:160114829 C>T maps to NM_025153.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr5:160031013 A>T maps to NM_025153.2 A1065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:160059347 G>A maps to NM_025153.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr5:159996669 C>T maps to NM_025153.2 V1257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr5:160047858 G>A maps to NM_025153.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr4:47559925 T>G maps to NM_020453.3 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:47570957 T>G maps to NM_020453.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:113514663 C>T maps to NM_032189.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr13:113459360 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:113479827 G>A maps to NM_032189.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:138867414 G>C did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:138908946 T>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:138857059 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:138869370 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:138882218 C>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:138870477 C>A did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr23:138878474 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:25284958 C>A maps to NM_001185085.1 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr13:25284995 C>A maps to NM_001185085.1 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:19762518 G>A maps to NM_020410.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:17331276 C>A maps to NM_022089.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:194151919 C>T maps to NM_024524.3 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:194147856 A>C maps to NM_024524.3 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:193183866 C>A maps to NM_032279.2 G407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:193183888 G>A maps to NM_032279.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:193232567 G>C maps to NM_032279.2 Y51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr3:193132515 T>A maps to NM_032279.2 K956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:193159352 C>A maps to NM_032279.2 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:193158356 G>A maps to NM_032279.2 Q837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:193130150 T>A maps to NM_032279.2 T1008T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr3:193039550 G>A maps to NM_198505.2 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:116940527 A>T maps to NM_000701.7 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:160100079 G>T maps to NM_000702.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:160093178 C>T maps to NM_000702.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:160098515 G>T maps to NM_000702.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:42485655 G>A maps to ENST00000441343 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:42490036 G>T maps to ENST00000441343 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:160143417 C>A maps to NM_144699.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:160137138 G>A maps to NM_144699.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:160147345 T>C maps to NM_144699.3 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:160129228 G>T maps to NM_144699.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:7556734 C>G maps to NM_001678.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:119509333 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:119504618 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:119500452 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:28913588 C>G maps to NM_173201.3 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:28914160 C>T maps to NM_173201.3 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:3846780 C>T maps to NM_174953.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:3850762 C>A maps to NM_174953.1 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:89992911 C>G maps to ENST00000428670 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr3:10392219 C>A maps to NM_001001331.2 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr3:10452491 C>T maps to NM_001001331.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:152814998 C>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:152845731 C>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:152818708 G>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:152823610 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:152827613 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:152818657 C>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:152821584 C>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:203652419 G>T maps to NM_001001396.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:130674958 C>T maps to NM_001001486.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:130682865 G>A maps to NM_001001486.1 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr3:130656304 C>T maps to NM_001001486.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr16:84492923 G>T maps to ENST00000416219 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr16:84486817 G>T maps to ENST00000416219 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:36050024 C>A maps to NM_000704.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:36050048 G>A maps to NM_000704.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr13:114307222 C>A maps to NM_000705.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:40450617 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:40642585 A>T maps to NM_001130020.1 K376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:124228438 C>T maps to NM_012463.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr7:138429989 G>A maps to NM_130840.2 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr5:172410955 T>G maps to NM_003945.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:149572731 C>G maps to NM_001100592.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:113528273 G>C maps to NM_001690.3 *618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr3:113524308 A>G maps to NM_001690.3 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr2:71188823 G>T did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr2:71185478 C>A maps to NM_001692.3 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr8:20055040 C>T maps to NM_001693.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr8:104054575 G>T maps to NM_001695.4 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:10912725 C>A maps to NM_001039362.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr22:18077342 T>G maps to NM_001696.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:54684612 C>A maps to NM_015941.2 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr8:54682287 G>C maps to NM_015941.2 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:77271289 T>A did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:77301841 A>G did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:77284911 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:77254001 C>A did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr23:77289123 G>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:77244008 C>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:77267091 C>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:77301850 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:77301960 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:52548332 G>T maps to NM_000053.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:52548914 G>A maps to NM_000053.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr13:52535997 A>G maps to NM_000053.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr13:52520500 C>T maps to NM_000053.2 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:42446600 C>T maps to NM_006095.2 W1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr4:42558041 A>G maps to NM_006095.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr4:42580396 G>T maps to NM_006095.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr4:42618095 C>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:42553230 G>T maps to NM_006095.2 S529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr13:26145829 G>A maps to NM_016529.4 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr13:26144966 T>G maps to NM_016529.4 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr18:55361813 C>T maps to NM_005603.4 T343T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3409-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:55398970 G>T maps to ENST00000420338 *155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:55362764 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:154316386 C>T maps to NM_020452.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:154316368 G>T maps to NM_020452.3 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr1:154316659 G>T maps to NM_020452.3 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:154317829 G>T maps to NM_020452.3 E868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:1791761 G>T maps to NM_138813.2 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr15:50264805 T>A maps to NM_024837.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:50271995 C>A maps to NM_024837.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr15:50271901 C>A maps to NM_024837.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr20:50221482 C>A maps to NM_006045.1 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:50221364 C>A maps to NM_006045.1 E1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr20:50342414 G>A maps to NM_006045.1 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr20:50273653 C>A maps to NM_006045.1 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr18:76936876 G>C maps to NM_198531.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr18:77119462 G>T did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:17942270 C>T maps to NM_145691.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:35834709 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:142272708 G>A maps to NM_001184.3 H830H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:142281928 C>A maps to NM_001184.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr3:142178211 T>A maps to NM_001184.3 T2402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr20:3543853 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:117061500 C>T maps to NM_207303.2 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr10:117226717 C>G maps to NM_207303.2 S1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:117221451 C>G maps to NM_207303.2 Y1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:117075193 C>A maps to NM_207303.2 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:117093819 C>T maps to NM_207303.2 C1022C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:116919864 C>A maps to NM_207303.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:117075229 C>A maps to NM_207303.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:76889175 G>C did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:76938689 C>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:76937557 C>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:76919045 T>C did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:76854944 C>G did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:76937344 T>A did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:76763843 T>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:76938925 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:76920165 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:76938171 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:76938657 T>C did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:76855028 T>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:76890177 C>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:76938247 C>T did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr12:111957680 A>T did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr16:28847340 C>T maps to NM_148414.1 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr16:28841355 G>C maps to NM_148414.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:92549497 C>A maps to ENST00000359819 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr14:92555161 C>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:13337086 T>C did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:13337108 T>C did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:13337076 C>G did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:13337593 G>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:63981633 A>G maps to NM_001177387.1 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:63938122 C>T maps to NM_001177387.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr1:110028701 A>T maps to NM_153340.4 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr17:42271945 A>G maps to NM_020218.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:42272025 C>A maps to NM_020218.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr20:54963222 C>A maps to NM_198437.1 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:70255477 G>A maps to NM_015570.2 R1092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:70255531 C>T maps to NM_015570.2 Y1110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:58200196 G>T maps to NM_006576.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:63544085 C>A maps to NM_000706.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:206224941 C>T maps to NM_000707.3 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:153171710 C>A did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:153171311 C>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:153171763 G>C did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:69262235 C>A did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr17:63526216 A>G maps to NM_004655.3 Y803Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr17:63554606 C>T maps to NM_004655.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr17:63554498 C>T maps to NM_004655.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr19:41744042 G>T maps to NM_021913.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:41726676 G>A maps to NM_021913.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr15:45007660 G>A maps to NM_004048.2 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr15:45007767 C>G maps to NM_004048.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:160804254 G>A maps to NM_033168.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:235647795 C>A maps to ENST00000366599 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:168726220 G>A maps to NM_020981.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:168726010 C>G maps to NM_020981.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:1168119 G>A maps to NM_080605.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr11:134253789 G>A maps to NM_054025.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr11:134253717 G>A maps to NM_054025.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:62449631 C>T maps to NM_006577.5 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:17922702 T>C maps to NM_014256.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr3:182988593 T>C maps to NM_032047.4 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:182987915 G>A maps to NM_032047.4 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:41932671 G>A maps to NM_198540.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:80963007 C>A maps to NM_001009905.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr17:47241535 G>T maps to NM_153446.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:657443 C>A maps to NM_173593.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr11:376310 C>T maps to NM_178537.4 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr9:33135351 C>G maps to NM_001497.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:44446939 C>T maps to ENST00000309519 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:44446879 G>A maps to ENST00000309519 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr20:48259097 C>T maps to NM_004776.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:177036617 G>T maps to NM_007255.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:117160475 A>G maps to NM_012104.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr21:42647527 C>T maps to NM_012105.3 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:90660399 G>T maps to NM_001170794.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr6:90660873 G>A maps to NM_001170794.1 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr10:121436370 G>T maps to NM_004281.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:38067631 C>A maps to NM_004874.2 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr14:104026792 C>A maps to NM_001015049.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr21:11097575 C>T maps to NM_182482.2 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:40751487 G>A maps to NM_014952.3 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:143560702 C>T maps to NM_001702.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr8:143603330 G>A maps to NM_001702.2 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr8:143545864 C>A maps to NM_001702.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr8:143614676 C>T maps to NM_001702.2 C1140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:32196406 G>T maps to NM_001703.2 S1458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:32198744 C>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:69653822 G>T maps to NM_001704.2 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:69653725 C>T maps to NM_001704.2 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr6:69758172 C>G maps to NM_001704.2 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr6:70049311 C>T maps to NM_001704.2 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:70082330 G>T maps to NM_001704.2 E1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:69759193 C>T maps to NM_001704.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:69949087 A>T maps to NM_001704.2 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr6:70037781 G>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:69703704 G>T maps to NM_001704.2 G594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:69666041 G>A maps to NM_001704.2 W441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:70071176 G>T maps to NM_001704.2 E1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr6:69653875 T>G maps to NM_001704.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr6:70070786 C>T maps to NM_001704.2 R1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr6:69653720 G>C did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr17:79082294 G>A maps to NM_017451.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:97991744 C>G did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr16:1394610 C>T maps to NM_003933.4 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:1396057 C>A maps to NM_003933.4 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:1398481 G>C maps to NM_003933.4 *1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr16:88052142 G>A maps to NM_001173543.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:88061217 C>A maps to NM_001173543.1 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr3:52443745 C>A maps to NM_004656.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:215617173 T>A maps to NM_000465.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:91182611 G>A maps to NM_020063.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:91177964 C>A maps to NM_020063.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:129321281 C>A maps to NM_003658.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr5:17275786 C>T maps to NM_006317.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:31498658 T>A maps to ENST00000417556 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:31590629 C>T maps to NM_080686.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:31599914 C>T maps to NM_080686.2 A1155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr6:31598560 G>A maps to NM_080686.2 E816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:134321842 G>C maps to NM_013318.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:134350752 G>T maps to NM_013318.3 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:134348895 A>G maps to NM_013318.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:171509442 A>G maps to ENST00000392078 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:171504700 C>T maps to ENST00000392078 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:171510561 G>C maps to ENST00000392078 L1319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:35240765 G>C maps to NM_013448.2 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:35295248 G>C maps to NM_013448.2 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr14:35280154 T>C maps to NM_013448.2 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:72903595 G>A maps to NM_032408.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:72865209 C>A maps to NM_032408.3 E1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr7:72891485 T>G maps to NM_032408.3 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr7:72865252 C>A maps to NM_032408.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:72907246 G>A maps to NM_032408.3 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:57000517 C>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr12:57008796 C>A did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:160303430 T>C maps to NM_013450.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:160255378 C>T maps to NM_013450.2 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:160304782 C>A maps to NM_013450.2 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:160205324 C>T maps to NM_013450.2 W1719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:160289370 G>C maps to NM_013450.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:47725146 G>A maps to NM_001127240.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:27148879 C>T maps to NM_003986.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:66287219 G>A did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr4:123663905 G>T maps to NM_152618.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr4:123665026 G>T maps to NM_152618.2 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr16:56548502 G>C maps to NM_031885.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr15:73028216 C>T maps to NM_033028.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:122749309 T>G maps to NM_176824.1 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:33427608 G>A maps to NM_198428.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr7:33573663 G>A maps to NM_198428.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr3:107435500 T>G maps to NM_001142568.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr3:107429439 G>T maps to NM_001142568.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr3:107492319 A>G maps to NM_001142568.1 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr3:107492022 C>T maps to NM_001142568.1 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:45317914 G>T maps to NM_005581.3 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:156618366 G>T maps to NM_021948.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:156626089 C>T maps to NM_021948.3 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr1:156618423 G>A maps to NM_021948.3 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr7:107224330 C>T maps to NM_001008405.2 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:152981079 G>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:152986425 A>G did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr16:75268933 C>G maps to NM_001170714.1 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr16:75269713 C>A maps to NM_001170714.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr20:52645089 G>A maps to NM_003657.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr20:52570114 C>T maps to NM_003657.2 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr20:52569970 C>A maps to NM_003657.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr17:59112075 G>T maps to ENST00000407086 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:59024695 G>T maps to ENST00000407086 G402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:127524683 C>G maps to NM_078468.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:165548176 T>C maps to NM_000055.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr3:165504056 G>A maps to NM_000055.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:165547522 G>A maps to NM_000055.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:41903743 G>T maps to NM_000709.3 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:41916684 G>A maps to NM_000709.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:80837261 A>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:60687766 G>A maps to NM_022893.3 H760H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:60687658 C>T maps to NM_022893.3 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:60679700 C>T maps to NM_138559.1 *244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:60688726 G>A maps to NM_022893.3 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:60773217 C>T maps to NM_022893.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:99642497 T>C maps to NM_138576.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr15:80263170 A>G maps to NM_004049.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr12:12232613 G>T maps to NM_138722.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr14:23777251 C>T maps to NM_004050.4 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:45262823 A>T maps to NM_005178.4 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:187449663 G>A maps to NM_001706.4 I72I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-66-2793-01A-01D-1267-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr17:6927750 C>T maps to NM_181844.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr16:30899245 T>A maps to NM_004765.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:147083633 C>G did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:118769594 G>A maps to NM_182557.2 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:136599154 C>T maps to NM_014739.2 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:136599222 G>A maps to NM_014739.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr6:136597501 T>C maps to NM_014739.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr6:136599454 T>C maps to NM_014739.2 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr6:136599750 G>T maps to NM_014739.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:136597387 A>T maps to NM_014739.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:136597354 G>T maps to NM_014739.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:136597414 G>T maps to NM_014739.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:81279094 G>A maps to NM_017429.2 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:81303771 C>T maps to NM_017429.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr16:81314535 A>G maps to NM_017429.2 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:39932856 G>T did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:39932784 G>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:39933449 G>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:39933801 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:39933921 G>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:39922015 C>G did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:39933861 T>G did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:39934378 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:39934137 C>G did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:129148792 C>G did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:129139247 G>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:129147551 C>T did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:129148944 G>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:129155068 A>T did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:129148207 A>C did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr23:129159313 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:129149113 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:129189939 G>T did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr22:23596019 C>T maps to NM_004327.3 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr3:197238876 G>A maps to NM_203315.2 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:96730834 G>A maps to NM_000710.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:96706781 C>T maps to NM_000623.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr5:70855848 A>C maps to NM_018429.2 G2427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr5:70806896 C>A maps to NM_018429.2 T1326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr5:70844516 A>G maps to NM_018429.2 P2251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:101010248 G>C maps to NM_020836.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:18189143 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:18195716 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:18183310 G>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:18213563 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:18230739 C>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:18189189 T>A did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr23:18198763 A>G did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr6:107391716 G>A maps to NM_001080450.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr4:42122173 A>T maps to NM_207406.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr4:42145883 G>A maps to NM_207406.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:42145769 A>G maps to NM_207406.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:49224680 T>C maps to NM_024603.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr6:56857267 C>T maps to NM_152731.2 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:61729984 C>T maps to NM_001139443.1 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr7:93623547 C>A maps to NM_005868.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:102318110 C>G did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:102317850 G>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:102317935 C>T did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:102471402 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:102471254 T>C did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr20:17492635 C>A maps to NM_001195.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:152773714 C>G did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:102005283 C>G did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:102004379 C>G did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr5:78423632 C>A maps to NM_001713.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:32459056 G>A did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr12:32490543 C>G maps to NM_001714.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr8:22488074 G>A maps to NM_018688.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr8:22481751 G>A maps to NM_018688.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr2:32712730 G>T maps to NM_016252.3 G2611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr2:32832613 A>T maps to NM_016252.3 T4721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:32820203 A>G maps to NM_016252.3 L4535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:32773075 C>T maps to NM_016252.3 L4324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:32738146 A>G maps to NM_016252.3 A3498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:32754742 A>G maps to NM_016252.3 T3982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:32774510 C>G maps to NM_016252.3 L4369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:32725072 G>A maps to NM_016252.3 S2976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:53793363 C>T maps to NM_033341.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr13:103460093 A>T maps to NM_017693.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr8:11412925 G>A maps to ENST00000427279 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr8:11420486 G>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr8:11421499 C>G maps to ENST00000427279 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:11415528 G>C maps to ENST00000427279 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr8:11403589 G>T maps to ENST00000427279 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:28614916 T>A maps to NM_000386.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr7:43843317 C>T maps to NM_000712.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:40964288 G>A maps to NM_000713.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:169356239 A>G maps to NM_003666.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:22615392 G>T maps to NM_005180.6 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:22049653 G>T maps to NM_006129.4 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:50658839 C>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:50659052 T>G did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr20:6759228 G>T maps to NM_001200.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:6750874 G>T maps to NM_001200.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr14:54417391 G>A maps to NM_130850.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:55684594 G>A maps to NM_021073.2 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr6:55739435 A>C maps to NM_021073.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:55739373 G>T maps to NM_021073.2 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr6:7862564 G>T maps to NM_001718.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:7862711 G>C maps to NM_001718.4 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:55803412 G>T maps to NM_001719.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:34118634 C>T maps to NM_133468.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:34097705 C>A maps to NM_133468.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:34182964 T>C maps to NM_133468.3 N623N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:34094842 T>C maps to NM_133468.3 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:43292045 G>T maps to NM_014753.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr10:43285799 G>T maps to NM_014753.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:43317571 G>A maps to NM_014753.3 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr10:43316086 G>A maps to NM_014753.3 R967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:15526550 T>C did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:15540663 C>G did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:15565026 C>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr15:83936915 A>G maps to NM_001717.3 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:16419454 G>A maps to NM_017637.5 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr9:16583007 G>A maps to NM_017637.5 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:16436262 C>T maps to NM_017637.5 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr15:59971938 C>T maps to NM_004330.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:151015541 C>T maps to NM_138278.3 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:112997104 G>T did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:112993495 G>C maps to ENST00000273395 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:13601317 C>G maps to NM_148894.2 V2402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr4:13603125 C>A maps to NM_148894.2 G1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr4:13605553 A>G maps to NM_148894.2 H990H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:13603498 T>C maps to NM_148894.2 E1675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:242511734 C>T maps to NM_032515.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr2:242511722 C>T maps to NM_032515.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:149871788 G>C maps to NM_016074.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:198640395 C>T maps to NM_197970.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr6:3152807 G>C maps to NM_004332.2 *292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr20:36953174 G>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr20:31629811 C>A maps to NM_174897.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr20:31622638 G>T maps to NM_174897.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:220253146 G>A maps to NM_006085.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:65925452 C>T maps to ENST00000321892 G2126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:65850531 C>T maps to ENST00000321892 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:65822266 G>T maps to ENST00000321892 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:140449219 T>C did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:140534435 G>C maps to NM_004333.4 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr7:140534645 T>C maps to NM_004333.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr12:112082155 T>A maps to NM_006768.3 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:41256905 G>A maps to ENST00000471181 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr17:41246320 T>A maps to ENST00000471181 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:41215390 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:41244069 T>A maps to ENST00000471181 K1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr13:32937314 G>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr13:32907109 C>T maps to NM_000059.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr13:32912925 A>G maps to NM_000059.3 L1478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr13:32930589 C>A maps to NM_000059.3 A2487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr13:32911359 A>G maps to NM_000059.3 K956K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr13:32914164 A>T maps to NM_000059.3 A1891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr13:32900677 G>T maps to NM_000059.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr13:32915253 T>C maps to NM_000059.3 F2254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:154299829 C>T did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr22:50170799 C>A maps to ENST00000342989 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:50216963 G>C maps to ENST00000342989 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr22:50191603 A>G maps to ENST00000342989 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr22:50217445 T>A maps to ENST00000342989 K174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr22:50216867 G>T maps to ENST00000342989 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:32944195 G>T maps to ENST00000395289 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr6:32947733 A>G maps to ENST00000395289 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:15349586 C>A maps to NM_058243.2 R1329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr19:15354076 G>A maps to NM_058243.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:15350262 T>G maps to NM_058243.2 P1172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:137506040 T>C maps to NM_139199.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:878483 C>A maps to NM_001009877.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:92441988 G>T maps to ENST00000347608 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:92430224 A>T maps to ENST00000347608 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:92441931 T>C maps to ENST00000347608 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:28521251 C>T maps to NM_004899.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr14:105692498 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:105739130 C>A maps to NM_001519.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr8:37704487 C>A maps to NM_018310.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:97920545 C>G maps to NM_015379.4 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:59761289 C>T maps to NM_032043.2 E1039E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:166780281 C>T did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr3:9786058 C>T maps to NM_001003694.1 H929H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:9788856 C>T maps to NM_001003694.1 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:9782561 G>T maps to NM_001003694.1 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:9784740 C>G maps to NM_001003694.1 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr3:9781411 C>T maps to NM_001003694.1 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:36172573 C>T maps to NM_015695.2 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:36193101 G>C maps to NM_015695.2 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:135570419 C>A did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:55813534 C>T maps to NM_032430.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr11:1466646 C>T maps to NM_003957.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:79971738 C>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:80047435 A>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:79978190 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:79974985 A>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:79975092 G>C did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:79999650 G>C did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:79999571 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:80064746 G>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:79946651 C>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:79936890 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:79937528 G>A did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:79945465 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:79978074 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:79999533 T>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:79999629 A>G did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:79932486 C>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:79975107 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:62472873 G>A maps to NM_001130702.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:49690810 C>T maps to NM_003458.3 S1274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:49698115 G>A maps to NM_003458.3 R2946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr3:49689523 G>T maps to NM_003458.3 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr3:49699828 C>T maps to NM_003458.3 A3517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:49689697 G>T maps to NM_003458.3 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr3:49698244 T>C maps to NM_003458.3 S2989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:55470714 C>T maps to NM_057176.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:55464891 C>T maps to NM_057176.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr9:116116563 T>A maps to NM_017688.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:93749177 C>T maps to NM_003972.2 Q899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr10:93768863 G>A maps to NM_003972.2 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:3633447 G>T maps to NM_032444.2 Y1601*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-4721-01A-01D-1441-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-56-6546-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:72356211 C>T maps to ENST00000440684 Q795*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-66-2787-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:93708945 C>T maps to NM_001002860.2 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:92546278 T>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:92546224 C>A maps to NM_183242.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:15643401 G>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:15677002 C>T maps to NM_000060.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr23:100615710 T>C did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:100611770 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:100630169 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:100611134 G>C did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:100613621 C>G did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:100611125 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:100611047 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:100617572 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:100630230 G>T did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:100604917 T>G did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr3:112198389 C>G maps to NM_181780.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr6:26505288 A>T maps to NM_001732.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:26506972 G>T maps to NM_001732.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:26468326 G>T maps to NM_007049.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:26391043 A>T maps to NM_001197237.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:26406242 G>A maps to NM_007048.5 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:26410259 C>A maps to NM_007048.5 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:26444263 C>T maps to NM_006994.4 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:26445990 G>T maps to NM_006994.4 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr6:26446184 G>T maps to NM_006994.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:32374846 G>A maps to ENST00000468270 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr5:180420134 G>A maps to NM_197975.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:180377021 G>A maps to NM_001040462.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:180475254 G>A maps to NM_152547.4 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:180477307 G>A maps to NM_152547.4 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr5:180486678 C>T maps to NM_152547.4 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:103281515 C>T maps to NM_033637.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:111425420 T>A maps to NM_004336.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr15:40477471 G>A maps to ENST00000412359 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr15:40498626 C>T maps to ENST00000412359 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:99013773 G>A maps to NM_003910.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:56387417 C>T maps to NM_004758.2 E1267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:16705106 G>T maps to NM_014038.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr10:98744527 A>G maps to NM_015652.2 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr10:127422225 G>A maps to ENST00000356792 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:127434417 G>A maps to ENST00000356792 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr10:127429672 T>C maps to ENST00000356792 N758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr10:21805146 C>T maps to NM_207371.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr10:5799559 T>C maps to NM_017782.4 D2270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr10:5789239 C>T maps to NM_017782.4 L1286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr10:104572553 C>T maps to NM_001083913.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr10:72531215 C>T maps to NM_152710.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:99995215 G>C maps to ENST00000314594 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr10:99994209 G>T maps to ENST00000314594 G671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:120514169 G>A maps to NM_153810.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr10:50916590 T>A maps to NM_182554.2 C134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr10:73521604 C>T maps to NM_022153.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:99350268 C>T maps to NM_001009997.2 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr10:33015719 A>G maps to ENST00000375025 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:33015710 C>G maps to ENST00000375025 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:50531520 T>C maps to NM_001135196.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr10:50531321 C>T maps to NM_001135196.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:50227711 C>A maps to NM_001031746.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:50315655 G>T maps to NM_001031746.3 S147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr10:103792913 G>A maps to NM_024541.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:105912412 C>T maps to ENST00000389588 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr10:120095117 C>T maps to NM_022063.2 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr10:124697584 C>A maps to NM_024942.3 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr10:124708164 C>G maps to NM_024942.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:128193389 C>A maps to NM_001004298.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr10:128150140 G>A maps to NM_001004298.2 C516C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr10:128147645 G>T maps to NM_001004298.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr10:128147612 C>G maps to NM_001004298.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:134743004 G>T maps to NM_173572.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:118084896 T>C maps to NM_198515.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:118084899 G>A maps to NM_198515.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:61557388 C>A maps to NM_014206.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:8947121 T>C maps to NM_020643.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:64875683 C>T maps to NM_013265.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr11:68030120 C>T maps to NM_022338.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:68029629 G>C maps to NM_022338.3 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:76255757 C>T maps to ENST00000393457 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:76171007 G>T maps to ENST00000393457 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:33566520 G>A maps to ENST00000389726 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:33682445 C>A maps to ENST00000389726 A1724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:33566886 G>T maps to ENST00000389726 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:33565037 C>T maps to ENST00000389726 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:33572686 G>C maps to ENST00000389726 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:33565883 T>A maps to ENST00000389726 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr11:33667413 G>A maps to ENST00000389726 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:47073975 C>T maps to NM_001003677.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:111156673 C>T maps to NM_198498.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:93494784 C>A maps to ENST00000354421 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:93483518 G>A maps to ENST00000354421 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr11:122756634 A>T maps to NM_024806.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr11:122795603 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:36654837 T>C maps to NM_138787.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:82644902 T>C maps to NM_145018.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:107364964 T>A maps to NM_152261.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:82780744 T>C maps to NM_032230.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr12:32137483 G>T maps to NM_018169.3 E1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:32138193 G>T maps to NM_018169.3 A1435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:32134683 A>G maps to NM_018169.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr12:32137041 A>T maps to NM_018169.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr12:32145369 A>G maps to NM_018169.3 L1715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:13526184 C>A maps to ENST00000318426 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr12:40037720 T>A did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:40020149 C>G maps to NM_001031748.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:49072820 T>A maps to NM_017822.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:102589748 G>T maps to NM_017915.3 G474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr12:102569287 G>T maps to NM_017915.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr12:4461509 G>T maps to NM_020375.2 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr12:112632707 G>A maps to NM_001109662.2 L2738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:112666056 C>T maps to NM_001109662.2 L2058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:112670831 C>T maps to NM_001109662.2 V1819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr12:112688129 C>A maps to NM_001109662.2 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:112654879 G>A maps to NM_001109662.2 P2226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr12:112686204 T>C maps to NM_001109662.2 E1182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:112669452 G>A maps to NM_001109662.2 Q1850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr12:112685956 G>A maps to NM_001109662.2 Q1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:97102581 G>A did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr12:97087547 C>T maps to ENST00000342887 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:97093756 C>A maps to ENST00000342887 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr12:97150339 G>T maps to ENST00000342887 G1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:97151343 C>G maps to ENST00000342887 S1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:31814952 A>G maps to NM_001135864.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:93100562 G>A maps to NM_001037671.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:110495091 C>T maps to NM_207435.1 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr12:110480254 C>T maps to NM_207435.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr12:25147248 A>T maps to NM_001101339.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr13:46946523 C>A maps to NM_025113.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr13:39587738 G>A maps to NM_025138.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr13:39603488 T>C maps to NM_025138.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr13:39596550 T>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr13:43358263 C>T maps to NM_182508.2 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr13:37269403 C>T maps to NM_203451.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:57103234 A>G maps to NM_017799.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr14:57092201 G>T maps to NM_017799.3 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:57072379 C>A maps to NM_017799.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:50101288 C>T maps to NM_018139.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:45706888 G>A maps to NM_018353.4 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr14:45687518 A>G maps to NM_018353.4 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr14:74824649 G>A maps to NM_018228.2 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:74824955 C>T maps to NM_018228.2 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr14:74824820 G>T maps to NM_018228.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:74825297 C>T maps to NM_018228.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr14:76633044 C>G maps to NM_017926.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr14:60581997 C>T maps to ENST00000404681 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr14:60582114 A>G maps to ENST00000404681 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:60591741 A>G maps to ENST00000404681 E951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:81259309 C>A maps to NM_152446.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:59951016 C>T maps to NM_144581.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:52471215 G>A maps to NM_016039.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr14:77294667 C>T maps to NM_194287.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:77327100 G>A maps to NM_194287.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:73958888 G>T maps to NM_024644.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr14:77844684 T>G maps to NM_001010860.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:77844288 C>G maps to NM_001010860.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:99183496 T>A maps to NM_182560.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:78234793 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:76488674 C>T maps to NM_052873.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr14:76549568 G>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr14:69262627 C>T maps to NM_207442.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:24772359 G>T maps to NM_174913.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr14:24772987 C>G maps to NM_174913.1 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr14:45373613 G>T maps to NM_001017923.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr14:45369748 T>G maps to NM_001017923.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr14:58598407 C>T maps to ENST00000438670 E569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:74516688 G>T maps to NM_025057.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr14:95932314 G>A maps to NM_152592.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:95934294 G>A maps to NM_152592.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:95932537 C>G maps to NM_152592.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr14:95921781 C>A maps to NM_152592.3 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr14:100793707 G>A did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr14:103574848 C>T maps to NM_001077594.1 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:103574789 G>T maps to NM_001077594.1 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:24921211 C>T maps to NM_018958.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:24921839 T>C maps to NM_018958.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:24922789 C>T maps to NM_018958.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:24921811 C>T maps to NM_018958.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr15:24923587 G>A maps to NM_018958.2 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr15:24921122 C>A maps to NM_018958.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr15:24921170 C>A maps to NM_018958.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr15:81436088 C>T maps to ENST00000458088 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr15:76452463 G>A maps to NM_152335.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr15:76430134 G>A maps to NM_152335.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:49882083 G>A maps to NM_152647.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:75499669 A>T maps to NM_015492.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr15:37100542 C>T maps to NM_001130010.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr15:36946307 T>C maps to NM_001130010.1 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr15:65885800 T>C maps to ENST00000420799 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr15:40633068 G>A maps to NM_207380.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr15:40627418 C>G maps to NM_207380.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr15:39544395 G>A maps to NM_207445.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr15:34649515 C>A maps to ENST00000438749 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr15:40544698 C>G maps to NM_001039905.1 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr15:73843355 T>C maps to NM_001042367.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:1400988 C>T maps to NM_001001410.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:81095314 G>T maps to NM_152337.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr16:67700142 C>T maps to NM_032140.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:31502155 T>A maps to NM_022744.2 *469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr16:19659205 T>G did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr16:19603128 A>G maps to NM_020314.5 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:67180994 C>A maps to NM_025187.3 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr16:4790470 C>T maps to NM_139170.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:49433125 C>T maps to NM_144602.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr16:67702131 C>T maps to NM_001012984.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:19718330 C>T maps to NM_001012991.2 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr16:5108553 C>T maps to ENST00000350219 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr16:3544562 G>A maps to NM_001080524.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr17:32906211 G>A maps to NM_207454.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:21147436 G>A maps to NM_152914.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:42744413 C>T maps to NM_001145080.2 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr17:72955975 C>T maps to NM_030630.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr17:10608830 G>C maps to NM_020233.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr17:42225980 G>A maps to NM_024032.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:34190508 G>A maps to NM_152781.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr17:34190545 C>T maps to NM_152781.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr17:34182400 A>T maps to NM_152781.2 L460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:8138498 C>T maps to NM_025099.5 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:79516347 C>G maps to NM_025161.5 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr17:79514178 G>A maps to NM_025161.5 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:57288252 C>A maps to NM_018149.6 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr17:72588709 G>A maps to NM_152460.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr17:30179202 G>A maps to NM_018405.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr17:3717727 A>G maps to NM_001114118.1 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr18:13621221 C>T maps to NM_181481.3 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:13438378 C>T maps to NM_181481.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr18:13671860 C>T maps to NM_152352.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:77805899 C>T maps to NM_024805.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr18:77794644 G>C maps to NM_024805.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr18:47010052 T>C maps to NM_001035005.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr18:30873190 C>A maps to NM_001105528.1 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr18:30825249 C>A maps to NM_001105528.1 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr18:51904606 G>A maps to ENST00000382911 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:30199260 C>T maps to NM_001031726.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:30505792 G>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr19:30505963 A>G maps to NM_003796.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:757476 G>T maps to NM_173481.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:758595 G>A maps to NM_173481.2 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr19:758683 G>T maps to NM_173481.2 E580*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-46-3769-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr19:40827974 A>C maps to ENST00000357884 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:51301372 C>T maps to NM_199249.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:18679272 G>T maps to NM_024069.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:41248483 G>A maps to NM_198476.3 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:7743011 C>A maps to NM_174918.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:50984168 C>T maps to ENST00000376920 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:51768733 C>A maps to NM_173635.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:51770707 A>G maps to NM_173635.1 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:68270066 G>T maps to ENST00000407324 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:119760289 A>G did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:119760818 C>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:22965843 C>T maps to NM_015991.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:22987626 C>T maps to NM_000491.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:22987581 C>T maps to NM_000491.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:22973780 C>A maps to NM_172369.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:22974056 G>A maps to NM_172369.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:77043890 G>T maps to ENST00000392445 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr22:37578344 G>T maps to NM_182486.1 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr22:37578617 G>A maps to NM_182486.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:15437384 T>C maps to NM_001135170.1 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:15437465 C>T maps to NM_001135170.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:15443951 G>C maps to NM_001135170.1 P140P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3421-01A-01D-0983-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-22-4604-01A-01D-1267-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr13:24466030 A>G maps to NM_001135816.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:7241891 T>A maps to ENST00000290575 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:7171670 C>T maps to NM_001734.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr12:7177908 G>A maps to NM_001734.3 W674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:111490703 G>A maps to NM_018372.3 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:111494389 T>A maps to NM_018372.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:111495193 T>C maps to NM_018372.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:155290667 G>A maps to NM_001039517.1 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:172414238 T>C maps to NM_139240.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:172417619 G>A maps to NM_139240.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:210001470 G>A maps to NM_014388.6 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:162344104 G>T maps to NM_182581.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:162343861 G>T maps to NM_182581.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:169798415 C>T maps to NM_018186.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:169775193 T>C maps to NM_018186.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:169390621 C>T maps to ENST00000367806 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:179380307 T>A maps to NM_144696.4 Y379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:179478446 G>A maps to NM_144696.4 W802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:179494491 G>A maps to NM_144696.4 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:11008316 T>C maps to NM_001170754.1 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:24113865 A>T maps to NM_020362.4 *212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:231374719 G>A maps to ENST00000421623 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:67558693 G>A maps to NM_001013674.1 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:67591440 G>C maps to NM_001013674.1 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr1:247719714 G>T maps to NM_145278.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr1:247712511 C>A maps to NM_145278.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:169762071 T>C maps to NM_033418.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:12820844 G>T maps to NM_152290.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:1021390 C>A maps to ENST00000448924 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:116670899 C>T maps to NM_152367.2 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:53153697 G>A maps to NM_023077.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr1:57224415 A>G maps to NM_001004303.4 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:27278629 C>T maps to NM_152365.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:27277974 G>A maps to NM_152365.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:75037157 C>T maps to NM_001002912.4 G1412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:75037712 C>G maps to NM_001002912.4 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:75036890 A>C maps to NM_001002912.4 P1501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:75114929 C>T maps to NM_001002912.4 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:75037022 T>A maps to NM_001002912.4 A1457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:75038489 G>A maps to NM_001002912.4 D968D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:75037415 T>A maps to NM_001002912.4 T1326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr1:75037756 C>A maps to NM_001002912.4 E1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:75086532 C>A maps to NM_001002912.4 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr1:3806598 G>A maps to NM_207356.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:55134562 C>T maps to ENST00000454855 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:11766365 G>T maps to NM_198545.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:161336227 C>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:230979362 C>A maps to NM_032800.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:36181835 T>A maps to NM_152374.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:162351744 C>T maps to NM_001135240.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:213009398 G>T maps to NM_001024601.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:185094121 A>C maps to NM_030934.4 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr1:185153959 C>G maps to NM_001105518.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:28209121 T>C maps to NM_001105556.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:226173191 C>G maps to NM_152608.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:226175616 C>A maps to NM_152608.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:156376973 A>G maps to ENST00000357975 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:16332411 A>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:16332705 C>T maps to NM_178840.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:223567977 G>C maps to NM_152610.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:223568430 G>A maps to NM_152610.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:228363081 C>T maps to NM_001010867.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:209956841 C>A maps to NM_152485.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr1:209956790 T>C maps to NM_152485.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:153617730 G>T maps to NM_015607.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:43870164 G>T maps to ENST00000310739 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:60476070 C>T maps to NM_152377.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:60538307 G>C maps to NM_152377.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:172520689 C>G maps to ENST00000367723 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:156902655 C>T maps to NM_144702.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:156897311 C>T maps to NM_144702.2 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:34667844 C>A maps to NM_001134734.1 T477T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-37-3783-01A-01D-1267-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:55100910 A>T maps to NM_001012971.3 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr20:54941159 C>T maps to NM_080821.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:61576135 G>T maps to NM_017896.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr20:31044085 G>A maps to NM_080616.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:35437023 G>A maps to NM_080627.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:35443705 G>A maps to NM_080627.2 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:35443717 G>C maps to NM_080627.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr20:35444581 C>T maps to NM_080627.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr20:35467802 C>A maps to NM_080627.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr20:35444017 G>T maps to NM_080627.2 C609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr20:18433326 C>A did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr20:35769623 G>T maps to ENST00000343811 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:60987707 C>T maps to NM_080833.2 R616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr20:44515305 G>T maps to NM_080608.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:31659914 G>A maps to NM_182658.1 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr20:31671224 A>G maps to NM_182519.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr20:31671638 C>A maps to NM_182519.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr20:62187600 C>A maps to NM_024059.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr20:20270956 T>C maps to ENST00000389655 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr20:20232367 C>A maps to ENST00000389655 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr20:3734751 C>A maps to NM_001039140.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:3802835 G>C maps to NM_018347.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr20:24950912 C>T maps to NM_020531.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr20:1161764 G>T maps to NM_018354.1 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr20:1161743 C>T maps to NM_018354.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr20:746112 G>A maps to NM_033409.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr20:746321 C>A maps to NM_033409.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr20:31805392 G>A maps to NM_178466.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr20:31814783 T>C maps to NM_178466.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:18794464 G>A maps to NM_178483.2 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr20:18794683 C>A maps to NM_178483.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr20:56735871 G>C maps to NM_178456.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:45950964 G>A maps to ENST00000443468 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:45953713 G>A maps to ENST00000443468 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr21:45564779 T>C maps to NM_004649.6 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr22:32097715 T>C maps to NM_173566.2 S2011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr22:37397982 C>T maps to NM_001163857.1 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr22:23962791 G>T maps to NM_016449.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:45595790 G>A maps to NM_001009880.1 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:118986932 C>G maps to NM_014807.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr11:73753100 G>C maps to ENST00000334126 L1886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:73748583 C>A maps to ENST00000334126 G1940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:73785375 G>A maps to ENST00000334126 Q1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:27803209 T>C maps to NM_032266.3 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:27800101 A>G maps to NM_032266.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:75933712 C>T maps to NM_003203.4 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:75923426 A>G maps to NM_003203.4 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:75899135 T>C maps to NM_003203.4 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr2:44617433 A>T maps to NM_024766.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:24261179 T>G maps to NM_025203.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr2:88828670 C>A maps to NM_152670.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:241829490 G>A maps to NM_001085437.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr2:99413923 C>T maps to NM_207362.2 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:99443446 C>T maps to NM_207362.2 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr2:99438710 C>A maps to NM_207362.2 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:37468857 C>T maps to NM_144736.4 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr2:37474645 A>T maps to NM_144736.4 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:232458018 G>A maps to NM_152614.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr2:232458558 C>T maps to NM_152614.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:47357336 G>T maps to NM_001163561.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:219232572 C>T maps to NM_198559.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:55435828 C>A maps to NM_152385.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:74785923 G>T maps to NM_138804.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:197672175 G>C maps to NM_213608.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:197674074 G>A maps to NM_213608.1 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:210888921 A>C maps to NM_152519.2 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:200790044 T>C maps to NM_153689.5 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:26802210 G>T maps to NM_001105519.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:29296931 T>G maps to NM_001029883.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:29294604 T>C maps to NM_001029883.1 K841K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:29296002 T>C maps to NM_001029883.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:29287799 G>T maps to NM_001029883.1 R1268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:29296851 C>T maps to NM_001029883.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:120069254 C>A maps to NM_001017927.2 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:170502593 C>T maps to NM_001085447.1 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:74041312 C>A maps to NM_001080474.1 Y269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:74043168 C>A maps to NM_001080474.1 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:74043429 C>T maps to NM_001080474.1 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:74043035 C>T maps to NM_001080474.1 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:209045986 T>C maps to NM_001099334.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:24413498 G>T maps to NM_001040710.1 *207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:242815302 C>T maps to NM_173821.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:242814309 C>T maps to NM_173821.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:242814654 C>G maps to NM_173821.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:242814880 G>T maps to NM_173821.2 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:63631374 G>A maps to NM_015910.4 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:63720002 G>T maps to NM_015910.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr2:63631450 A>C maps to NM_015910.4 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:63609191 G>T maps to NM_015910.4 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:85051321 C>T maps to ENST00000409520 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:6697785 G>A maps to NM_000064.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:6696667 C>T maps to NM_000064.2 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr19:6684438 G>A maps to NM_000064.2 Q1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr12:8211895 G>A maps to NM_004054.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:8212270 T>A maps to NM_004054.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:119465999 A>G maps to NM_033364.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:112727208 C>G maps to NM_015412.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:50602962 C>A maps to NM_001171741.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:14695955 C>G maps to NM_016474.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr3:14744710 G>T maps to NM_032137.4 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:194991424 C>T maps to NM_152531.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:194991427 G>A maps to NM_152531.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr3:194877185 T>A maps to NM_152531.4 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:44409197 C>A maps to NM_173826.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:10146191 C>T maps to NM_001164839.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:99895186 C>T maps to NM_032359.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:128292466 G>A maps to NM_007354.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:118865206 A>T maps to NM_152539.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr3:155493632 G>C maps to ENST00000340171 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr3:196434642 C>A maps to NM_032898.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:129007815 C>A maps to NM_001006109.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr3:88205460 G>A maps to NM_173824.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:43121435 G>T maps to NM_032806.4 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr3:50324114 G>A maps to NM_153215.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:143691416 C>A maps to NM_173552.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr3:143691761 C>T maps to NM_173552.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr3:49314134 C>T maps to NM_198562.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:56681053 G>A maps to ENST00000447900 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:56680634 C>T maps to ENST00000447900 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:58849463 C>T maps to ENST00000482387 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:138669272 C>T maps to NM_001040061.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:207297616 C>T maps to NM_000715.3 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr4:57842860 C>A maps to NM_032313.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr4:100460362 G>A maps to NM_032149.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr4:37592255 C>A maps to NM_018302.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:113540354 T>C maps to NM_018392.4 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr4:113539911 G>C maps to NM_018392.4 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:113483615 A>G maps to NM_018392.4 C1536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:113540012 A>G maps to NM_018392.4 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:113524747 C>A maps to NM_018392.4 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:121966947 G>A maps to NM_024574.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr4:121961196 C>G maps to NM_024574.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:71201724 C>T maps to NM_033122.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:71201571 C>A maps to NM_033122.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:71201607 T>A maps to NM_033122.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:71201256 G>A maps to NM_033122.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:98893522 G>A maps to NM_174952.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr4:165878494 G>T maps to NM_153027.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr4:184626195 G>T maps to NM_021942.4 E1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr4:3251170 G>T maps to NM_001042690.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:5966795 G>A maps to ENST00000324058 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:146617715 C>G maps to NM_001080531.1 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr19:47823171 C>T maps to ENST00000355085 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:133295550 T>A maps to NM_020199.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr5:31538615 G>A maps to NM_018356.2 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr5:31538492 A>G maps to NM_018356.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:43446437 G>A maps to NM_022483.4 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr5:43446644 G>C maps to NM_022483.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr5:139622977 C>G maps to NM_032412.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:43506175 G>T maps to NM_198566.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr5:43506364 A>G maps to NM_198566.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr5:43506460 G>A maps to NM_198566.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:2752746 C>G maps to NM_178569.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:154199910 C>A maps to NM_032385.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:172513616 C>T maps to NM_153607.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr5:37169395 C>A maps to NM_023073.3 G2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:7832091 G>T maps to NM_001089584.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:41909864 A>T maps to NM_175921.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:41149418 C>T maps to NM_001115131.1 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:41172357 G>T maps to NM_001115131.1 C420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr5:41181586 T>C maps to NM_001115131.1 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:41181508 G>T maps to NM_001115131.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:41160346 A>G maps to NM_001115131.1 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:41143067 G>T maps to NM_001115131.1 C888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr5:41142974 A>T maps to NM_001115131.1 C919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:41160379 G>A maps to NM_001115131.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr6:32261408 T>C maps to ENST00000447241 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr6:32261378 C>T maps to ENST00000447241 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr6:11723605 C>A maps to NM_001143948.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:165715740 G>A maps to NM_144980.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:165715432 G>T maps to NM_144980.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr6:165715150 A>G maps to NM_144980.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr6:165711503 G>A maps to NM_144980.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:41037853 C>A maps to NM_145063.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr6:47847000 G>A maps to NM_001013732.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:54025349 G>T maps to ENST00000502396 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:31079765 C>A maps to NM_014070.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:31079487 C>A maps to NM_014070.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:31079658 G>T maps to NM_014070.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:43475242 C>T maps to NM_001012974.1 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr6:88125495 G>T maps to NM_001031743.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:97715857 G>A maps to NM_198468.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:97681742 C>T maps to NM_198468.2 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:121577238 T>C maps to ENST00000275159 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:121577250 A>G maps to ENST00000275159 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:127797193 C>A maps to NM_001012279.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr6:127797340 C>A maps to NM_001012279.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:133100532 T>A maps to NM_052831.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr6:118887132 T>C maps to NM_001042475.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr6:118887126 T>C maps to NM_001042475.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr6:151773688 C>A maps to NM_024573.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr6:36298395 G>C maps to NM_001010903.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr6:112420590 G>T maps to NM_001033564.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:42858256 C>G maps to NM_001008739.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr6:31691946 G>A maps to NM_138272.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr6:170169793 G>A maps to NM_018341.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr6:149903650 C>T maps to NM_138785.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr6:149893446 A>C maps to NM_138785.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:149901831 C>G maps to NM_138785.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:36870106 C>A maps to NM_152734.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:151917550 G>T maps to ENST00000367290 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:151894541 C>A maps to ENST00000367290 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:40947702 G>T did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr5:40936548 C>T maps to NM_000587.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr5:40981569 C>T maps to NM_000587.2 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:40950039 C>G maps to NM_000587.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr5:40981578 G>A maps to NM_000587.2 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:40220564 A>G maps to NM_001193311.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:40899990 C>T maps to NM_001193311.1 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:31746858 G>T maps to NM_006658.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:2580983 G>A maps to NM_152743.3 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr7:142637535 G>A maps to NM_178829.4 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:66416109 G>A maps to NM_017994.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr7:99754530 C>T maps to NM_018275.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr7:100815719 C>A maps to NM_198571.2 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr7:48086125 C>T maps to ENST00000430738 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:48083168 G>A maps to ENST00000430738 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:120629924 G>T did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr7:120911348 G>A maps to NM_024913.4 Q911Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr7:120884319 C>A maps to NM_024913.4 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr7:112535724 T>A maps to NM_152556.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:112579793 C>A maps to NM_152556.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr7:112472714 T>G maps to NM_152556.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:89937161 G>T maps to NM_001039706.2 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:92166181 A>T maps to NM_032120.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:47698585 G>A maps to NM_001123065.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:108524211 G>T maps to NM_001024607.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:6370350 G>A maps to NM_001037163.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:57349308 A>T maps to NM_000562.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:57351625 A>T maps to NM_000562.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr1:57372361 G>A maps to NM_000562.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:57415410 G>A maps to NM_000066.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:57395226 G>A maps to NM_000066.2 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr8:49985440 C>T maps to NM_001007176.3 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:69688633 G>T maps to NM_052958.2 G469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr8:69552747 T>A did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr8:69728118 A>G did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr8:10532250 C>A maps to NM_001040032.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:124232362 C>A maps to NM_032847.1 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:12879024 T>C maps to NM_020844.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr8:117950628 C>T maps to NM_001025357.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr9:98683537 C>T maps to NM_001010895.2 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr9:27284753 C>T maps to NM_020641.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:130473729 G>A maps to NM_001012502.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:131048233 G>T maps to NM_001040011.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr9:7799632 C>A maps to NM_033428.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr9:104238558 C>A maps to NM_032342.1 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr9:35819992 G>C maps to NM_001012446.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr9:35825344 A>T maps to NM_001012446.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr9:35045208 C>A maps to NM_203299.2 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr9:72459522 G>T maps to NM_001010940.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr9:135357712 C>A maps to NM_207417.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:139741706 C>G maps to NM_001080482.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:140146504 C>G maps to ENST00000388931 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:34610924 C>A maps to NM_148179.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr9:34382826 G>T maps to NM_032596.3 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr9:97522148 G>T maps to NM_001193329.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:86559727 T>A maps to NM_032307.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:27567112 C>T maps to NM_018325.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr9:90501471 T>C maps to NM_178828.4 D690D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr9:90501369 T>A maps to NM_178828.4 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr9:90503241 C>A maps to NM_178828.4 G1280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr9:90500688 G>A maps to NM_178828.4 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:90500667 C>A maps to NM_178828.4 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr9:90500145 G>A maps to NM_178828.4 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr9:90502146 C>A maps to NM_178828.4 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr9:90497820 C>T maps to NM_178828.4 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr9:90503379 C>A maps to NM_178828.4 I1326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:26884874 C>A maps to NM_024828.3 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr9:74526734 A>T maps to NM_182505.3 K29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr9:74526682 C>A maps to NM_182505.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:139733426 C>T maps to NM_001173988.1 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr9:95872956 C>T maps to NM_032310.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr9:95872920 G>A maps to NM_032310.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:117400948 C>T maps to ENST00000374049 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr9:15777728 G>T maps to NM_173550.2 E935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:15848935 G>T maps to NM_173550.2 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr9:15745612 C>T maps to NM_173550.2 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:135702385 G>C maps to NM_152572.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:50008433 C>T maps to NM_001082534.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:50149696 G>A maps to NM_001082534.1 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr17:49731085 G>T maps to NM_001082534.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:50008414 C>A maps to NM_001082534.1 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:86163131 C>T maps to NM_198584.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr8:86356351 G>T maps to NM_005181.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr8:86354333 C>T maps to NM_005181.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:87960507 G>A maps to NM_001739.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:15793397 A>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:15768282 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:66881130 G>A did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr8:61135249 G>T maps to NM_004056.4 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr22:24573529 G>A maps to NM_012295.3 E2088E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr22:24487754 C>A maps to NM_012295.3 I1248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:24483604 C>G maps to NM_012295.3 S1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr20:60969314 C>T maps to NM_031215.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:60967461 C>T maps to NM_031215.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:60967491 G>A maps to NM_031215.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:121098003 C>T maps to NM_001033677.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:121098053 C>T maps to NM_001033677.1 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:48547116 C>A maps to NM_019855.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr18:21723345 A>G maps to NM_138644.1 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:65120428 A>C maps to ENST00000371073 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr19:13616886 G>T maps to NM_023035.2 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:13476129 C>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr9:140772527 C>A maps to ENST00000277549 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:140809199 C>T maps to ENST00000277549 I239I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-66-2754-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:2602440 C>A maps to NM_199460.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr12:2602440 C>T maps to NM_199460.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:2775902 G>A maps to NM_199460.2 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:2721166 C>G maps to NM_199460.2 A1292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:2676921 C>G maps to NM_199460.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:2694566 G>T maps to NM_199460.2 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:2721172 A>G maps to NM_199460.2 K1294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:2676867 G>T maps to NM_199460.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr12:2224642 C>A maps to NM_199460.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr3:53787696 A>T maps to NM_001128840.1 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr3:53844042 G>A maps to NM_001128840.1 Q1970Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr3:53842703 G>A maps to NM_001128840.1 E1926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:181702137 G>A maps to ENST00000357570 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:181753904 G>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:181767669 G>C maps to ENST00000357570 P2214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:181620508 G>A maps to ENST00000357570 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:181764044 C>A maps to ENST00000357570 R2025R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:181726097 C>T maps to ENST00000357570 R1389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:181727123 C>A maps to ENST00000357570 T1457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:181549845 C>A maps to ENST00000357570 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:181707531 G>A maps to ENST00000357570 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:49087003 G>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:49065031 C>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:49075165 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:49086834 C>A did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:49067837 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:49068373 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:49074998 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:49066419 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:49065138 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:49079263 A>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:49076219 C>G did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr17:48655852 G>A maps to NM_018896.3 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr17:48674005 C>T maps to NM_018896.3 A1021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:48687293 C>G maps to NM_018896.3 S1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:48669395 C>A maps to NM_018896.3 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr16:1260848 G>T maps to NM_021098.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:1257786 C>T maps to NM_021098.2 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr16:1250519 C>T maps to NM_021098.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr16:1262138 G>A did not map to a codon.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr22:40060850 C>T maps to NM_021096.3 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr22:40045839 C>A maps to NM_021096.3 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:201021733 G>T maps to NM_000069.2 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:201047032 G>T maps to NM_000069.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr1:201030448 G>C maps to NM_000069.2 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:201044686 G>T maps to NM_000069.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:201047026 C>G maps to NM_000069.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:201060807 G>A maps to NM_000069.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:81591297 G>A maps to NM_000722.2 Q960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:82072710 G>T maps to NM_000722.2 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:81589145 C>A did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:81624183 C>T maps to NM_000722.2 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr3:50402575 G>C maps to ENST00000435965 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:2022269 C>T maps to NM_172364.4 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:1995535 G>A maps to NM_172364.4 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:1987507 G>T maps to NM_172364.4 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr12:49221639 G>A maps to NM_000725.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:152727092 C>T maps to NM_000726.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr16:24373168 C>T maps to NM_006539.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr17:64876809 C>A maps to NM_014404.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:54418652 C>G maps to NM_031896.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr19:54485586 G>T maps to NM_031895.5 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr2:27456573 T>C maps to NM_004341.3 N1099N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr2:27445785 C>T maps to NM_004341.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:115102103 G>A maps to NM_014333.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr3:86010797 G>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:159169595 C>T maps to NM_021189.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:44127511 T>C maps to NM_145296.1 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:44128311 G>A maps to NM_145296.1 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:44131918 C>A maps to NM_145296.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:62518604 G>A maps to ENST00000383709 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:62423865 G>T maps to ENST00000383709 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr3:62477986 C>T maps to ENST00000383709 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:62388830 G>A maps to ENST00000383709 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr3:62570894 G>T maps to ENST00000383709 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:62423877 C>T maps to ENST00000383709 G1231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:62739268 G>T maps to ENST00000383709 Y245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:62522230 G>A maps to ENST00000383709 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:122130222 G>T maps to NM_001167940.1 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr7:122047602 G>A maps to NM_001167940.1 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:122261628 A>C maps to NM_001167940.1 L337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:122114482 G>A maps to NM_001167940.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:7355338 T>C maps to NM_001170692.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:7373308 G>T maps to NM_001170692.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:91072418 G>C maps to NM_004929.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr16:71417889 G>A maps to NM_001740.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr12:54115396 C>G maps to NM_020898.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr12:54118510 C>A maps to NM_020898.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:46925693 G>T maps to ENST00000448105 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr17:46925691 C>T maps to ENST00000448105 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:93098043 C>T maps to NM_001164737.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr7:93116263 C>T maps to NM_001164737.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:93106912 G>T maps to NM_001164737.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr2:188210985 A>T maps to NM_005795.4 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr7:134617823 C>A maps to NM_033138.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:71488693 G>T maps to NM_031468.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr7:71571273 G>A maps to NM_031468.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:71252807 A>G maps to NM_031468.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:71252798 C>A maps to NM_031468.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:13049501 A>G maps to NM_004343.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:13054427 G>A maps to NM_004343.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:13051632 G>T maps to NM_004343.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:128399069 C>A maps to ENST00000342367 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:9803339 G>C maps to NM_003656.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:12856242 G>T maps to NM_153498.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:209785330 G>A maps to NM_020439.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:44323772 C>T maps to NM_001220.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:114378621 G>A maps to ENST00000515496 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:75620620 G>T maps to ENST00000423381 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr5:110809030 T>C maps to NM_001744.4 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:3779582 C>A maps to ENST00000381771 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr12:121690484 T>A maps to NM_006549.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr12:121686467 C>A maps to NM_006549.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:49899590 G>A maps to NM_024046.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:134076786 C>T maps to NM_001745.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr1:200784771 G>A maps to ENST00000236925 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:7724961 G>A maps to NM_015215.2 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:7792646 G>C maps to NM_015215.2 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:7724859 C>T maps to NM_015215.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:12861609 C>T maps to NM_001162499.1 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr17:76993182 A>G maps to NM_138793.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr17:76989727 G>T maps to NM_138793.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:179135999 T>C maps to ENST00000415618 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:85628386 G>C maps to NM_001747.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:85628713 C>A maps to NM_001747.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:85628768 G>C maps to NM_001747.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:241536286 C>T maps to NM_023083.3 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:241528824 G>C maps to NM_023083.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:31010095 G>T maps to ENST00000295055 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:30998885 C>A maps to ENST00000295055 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:223958165 C>A maps to NM_001748.4 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:42652293 C>T maps to NM_000070.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:76826624 G>A maps to ENST00000360841 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:76831860 G>T maps to ENST00000360841 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:110494321 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:110497518 T>C did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:110491096 A>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:110490676 G>T did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:110491960 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:110491796 C>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:110491217 T>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:110494146 G>T did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:110491209 G>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:110490619 G>A did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr1:230903310 G>A maps to NM_006615.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:30868012 G>A maps to NM_001002259.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:30873819 T>C maps to NM_001002259.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr12:30888128 C>G maps to NM_001002259.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:35921195 T>A maps to NM_144647.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:113189873 G>T maps to NM_006135.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr12:18891941 T>A maps to NM_033328.2 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:18891504 G>A maps to NM_033328.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr7:2987232 G>A maps to NM_032415.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr17:78179366 G>A maps to NM_024110.2 Q869Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:104912297 A>G maps to NM_001017534.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:105009761 C>A maps to NM_021571.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:105009723 A>T maps to NM_021571.3 L30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr5:40852858 C>T maps to NM_032587.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr5:40852399 A>T maps to NM_032587.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:40852846 C>G maps to NM_032587.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr5:40843653 G>T maps to NM_032587.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:40852717 G>T maps to NM_032587.3 V428V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3414-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr11:67191122 T>A maps to NM_001166222.1 L635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr11:3047974 C>A maps to NM_001014437.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:3022363 G>A maps to NM_001014437.2 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr13:111340109 C>A maps to NM_024537.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:94173842 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:41495860 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:41437648 C>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:41383257 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:2236735 G>A maps to NM_020764.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr16:2233645 C>A did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr16:2234822 A>C maps to NM_020764.3 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr11:104899949 C>A maps to NM_033292.2 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr19:15164417 C>A maps to NM_012114.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr19:15166250 C>A maps to NM_012114.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr7:142989493 C>T maps to NM_032982.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:143000959 G>T maps to NM_032982.2 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:104820345 G>A maps to NM_001225.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:104869684 C>T maps to NM_001136112.1 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr11:104879647 G>A maps to NM_001136112.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr10:115486074 G>C maps to NM_033338.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:202149560 A>G maps to NM_001080125.1 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr2:202149859 C>G maps to NM_001080125.1 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:202136258 C>G maps to NM_001080125.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:90575900 G>A maps to NM_012115.3 R964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:15844887 C>A maps to NM_001229.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:15833531 G>A maps to NM_001229.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr3:122003470 C>T maps to NM_001178065.1 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:122003494 G>T maps to NM_001178065.1 R908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr3:121980409 C>T maps to NM_001178065.1 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:55027179 A>T maps to NM_020356.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:55027971 C>T maps to NM_020356.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr20:55033730 G>T maps to NM_020356.3 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr20:55027083 T>C maps to NM_020356.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr20:55026900 G>A maps to NM_020356.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr20:55027875 G>A maps to NM_020356.3 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:96076485 C>A maps to ENST00000508830 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:10720207 G>A maps to NM_001079843.1 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:10716793 C>G did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:10699643 G>A maps to NM_001079843.1 A1545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:65786373 C>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr11:65786338 C>T maps to NM_053054.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:134305627 G>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:26524859 C>A maps to NM_198137.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:92105439 C>T maps to NM_024764.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:92185771 T>A maps to NM_024764.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr14:92088264 A>G maps to NM_024764.2 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr19:38847170 G>T maps to NM_021185.4 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:38851186 G>A maps to NM_021185.4 W556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr16:67116118 G>T maps to NM_022845.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:119103294 A>G maps to NM_005188.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:119103222 G>A maps to NM_005188.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:119149392 C>A maps to NM_005188.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:119155952 C>A maps to NM_005188.2 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:105495384 G>A maps to NM_170662.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr19:45284514 T>C maps to NM_012116.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr16:49315322 C>A maps to NM_004352.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:70209050 G>A maps to NM_182511.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr20:54578951 G>A maps to NM_080617.4 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:44492174 C>T maps to ENST00000398168 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr9:69238317 T>A did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr17:77757694 G>T maps to NM_005189.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr17:77808066 C>G maps to NM_003655.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr22:39262444 G>A maps to NM_014292.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:14029607 C>A maps to NM_017721.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:52824023 C>A maps to NM_032449.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:52821928 C>T maps to NM_032449.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:15529080 C>T maps to NM_001080522.2 Y387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:70502186 C>T maps to NM_018237.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:70509416 C>T maps to NM_018237.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr10:70513632 A>G maps to NM_018237.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr18:57103261 C>A maps to NM_133459.3 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr9:131597802 G>T maps to NM_004059.4 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:89418829 G>C maps to NM_001008661.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:89414822 G>A maps to NM_001008661.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:28592407 C>G maps to NM_138414.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr16:57546760 G>A maps to NM_033212.3 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr18:66513658 G>C did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr18:66678274 A>T maps to NM_024781.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr18:66504389 G>T maps to NM_024781.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr18:66504605 G>A maps to NM_024781.2 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr19:15131287 C>T maps to NM_173482.2 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr19:15132724 C>A maps to NM_173482.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:219895544 G>A maps to NM_194302.2 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:219903117 G>T maps to NM_194302.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr2:219903728 C>T maps to NM_194302.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:219878061 C>A maps to NM_194302.2 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:74631133 G>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:186379984 C>A maps to NM_152775.3 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr16:58287930 G>T maps to NM_014157.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:48806032 G>T maps to NM_144577.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:48801294 A>G maps to NM_144577.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr19:48807009 G>C maps to NM_144577.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:21991154 C>T maps to NM_152612.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr22:21988720 T>C maps to NM_152612.2 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr22:21989176 G>A maps to NM_152612.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:21990875 C>T maps to NM_152612.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:48922152 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:33392319 T>A did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr5:68616151 C>A maps to NM_176816.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr7:31611725 C>T maps to NM_194300.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:31618017 C>A maps to NM_194300.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:31592799 G>T maps to NM_194300.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:31682966 A>G maps to NM_194300.2 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr7:92983067 A>G maps to NM_017667.2 V860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr7:92905596 C>T maps to NM_017667.2 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:92978022 G>A maps to NM_017667.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr7:92985379 C>T maps to NM_017667.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:57732911 C>T maps to NM_032269.5 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:57732936 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:128452221 C>T maps to NM_022742.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:128446912 G>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:123634000 T>A maps to NM_022757.4 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr3:123650001 C>A maps to NM_022757.4 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:123665976 C>A maps to NM_022757.4 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179736943 G>A maps to NM_173648.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:179734014 A>T maps to NM_173648.3 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr2:179718285 G>T maps to NM_173648.3 C1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:179730514 G>T maps to NM_173648.3 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:179718258 G>T maps to NM_173648.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr17:16612187 C>T maps to NM_014695.1 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:16593971 A>G maps to NM_014695.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:18525828 G>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:106121840 G>T maps to NM_001008723.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:159107381 C>A maps to NM_138803.3 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:124875009 A>G maps to NM_025004.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:197593927 C>T maps to NM_001080539.1 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:197521509 C>G maps to NM_001080539.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:197577398 A>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:197541355 G>A maps to NM_001080539.1 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:11537556 C>G maps to NM_145045.4 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:11533514 C>A maps to NM_145045.4 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:11537595 C>T maps to NM_145045.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:119063870 C>T maps to NM_001145018.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:49916241 G>A maps to NM_144688.4 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr22:30772727 C>A maps to NM_001017437.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr22:30766589 G>A maps to NM_001017437.2 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr4:77290598 G>A maps to NM_001042784.1 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr4:77276502 C>A maps to NM_001042784.1 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr19:11460626 G>A maps to ENST00000427879 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:133379768 A>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:46088751 C>A maps to NM_001114938.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:93704968 C>A maps to NM_206886.2 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr1:93651975 G>A maps to NM_206886.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:26596024 C>T maps to NM_022778.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr1:26595017 C>T maps to NM_022778.2 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:49099759 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:49105370 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:49104771 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:3679829 G>A maps to NM_152492.2 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:3686366 G>A maps to NM_152492.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:3669364 T>C did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr1:3672111 C>A maps to NM_152492.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr1:3669113 C>A maps to NM_152492.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:139094849 G>A maps to NM_015439.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:32669965 C>T maps to ENST00000421922 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:74564126 G>A maps to ENST00000321288 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr15:74559106 C>T maps to ENST00000321288 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr15:74554867 G>A maps to ENST00000321288 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr3:49294147 T>C maps to NM_178173.3 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:126138989 C>A maps to ENST00000505024 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr3:126152022 C>T maps to ENST00000505024 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:180359791 C>T maps to NM_181426.1 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr3:180377269 C>T maps to NM_181426.1 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr17:78071153 C>T maps to NM_017950.2 F1044F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:78073441 C>G maps to NM_017950.2 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr17:78058645 G>A maps to NM_017950.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr17:78023867 G>T maps to NM_017950.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr17:8638527 G>T maps to NM_144681.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:63923747 C>T maps to NM_145036.3 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr17:61838332 T>A maps to NM_020198.2 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:61842098 C>G did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr3:128757706 C>T maps to NM_024768.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:191075832 G>A maps to NM_178335.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr3:113169254 G>A maps to NM_144718.3 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:107097324 T>G maps to NM_032600.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:107097231 C>A maps to NM_032600.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr12:119866544 A>T maps to NM_178499.3 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr19:46498681 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:123265747 C>G maps to NM_201435.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:123282702 G>A maps to NM_201435.3 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:49298763 G>A maps to NM_033124.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:56627032 G>C maps to NM_001141947.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:150578599 G>A maps to NM_015621.2 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:32856632 C>T maps to NM_001026383.1 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr13:52440011 G>A maps to NM_031290.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr3:48481714 C>T maps to NM_015933.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:32635289 G>A maps to NM_001008391.2 F858F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:32697137 T>C maps to NM_001008391.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:46914554 G>A maps to NM_032040.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:46915712 G>A maps to NM_032040.3 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:46914864 T>C maps to NM_032040.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr3:112357185 C>A maps to ENST00000447230 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:112357102 C>T maps to ENST00000447230 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr3:112358446 C>T maps to ENST00000447230 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:86111843 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:96117807 G>C maps to NM_024725.3 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr11:85610059 T>C did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr11:85584263 A>T maps to NM_173556.3 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:56419917 C>T maps to NM_001080433.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:56420270 G>T maps to NM_001080433.1 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr11:66358539 C>A maps to NM_018219.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:55562300 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64109192 G>A maps to NM_032251.5 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64121475 G>A maps to NM_032251.5 K1311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:64124515 G>T maps to NM_032251.5 E1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr14:91792394 C>T maps to NM_001080414.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr11:85396969 G>A maps to NM_152723.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:85396051 T>A maps to NM_152723.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:85397008 C>A maps to NM_152723.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr6:13802566 G>A maps to NM_001031713.2 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:118715997 G>C maps to NM_019044.4 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:41825635 C>T maps to NM_052848.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:169018200 A>T maps to NM_017785.4 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:31112994 C>T maps to NM_001105564.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:31112668 G>T maps to NM_001105564.1 Y686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:36170236 C>A maps to NM_005893.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:26483346 C>A maps to NM_000730.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr11:6291980 C>T maps to NM_176875.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:6290903 G>T maps to NM_176875.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr11:6291935 C>T maps to NM_176875.2 Y238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:57449012 C>A maps to NM_002987.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr2:228678677 A>C maps to NM_004591.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:75442679 G>A maps to NM_002991.2 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr7:75401208 C>A maps to NM_006072.4 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:75401322 T>A did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr17:34431318 C>G maps to NM_002984.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:45113070 A>G maps to NM_001029835.2 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr7:45112368 G>T maps to NM_001029835.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:68470109 G>C maps to NM_031966.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr5:68473064 G>C did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:50090770 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:50089750 T>A did not map to a codon.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr23:50037926 C>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:50094327 C>A did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:50052358 G>C did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr23:50052551 A>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:50054015 A>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:50051879 A>C did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:50053411 C>T did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:50051611 C>G did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:50051888 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:50052095 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:50054315 G>C did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:50094350 T>C did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:50055567 G>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:99997414 G>A maps to NM_005190.3 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr12:4385367 C>A maps to NM_001759.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr12:4383319 T>C maps to NM_001759.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr15:43484983 C>T maps to NM_012142.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:43483667 G>T maps to NM_012142.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:30308041 A>G did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:86695248 C>T maps to NM_001239.3 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:99968654 C>T maps to ENST00000437596 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr15:55652653 G>T maps to ENST00000442196 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:55651989 G>A maps to ENST00000442196 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:46244913 G>A maps to NM_001295.2 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr3:32994961 C>A maps to NM_005508.4 Y16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr3:46414527 T>C maps to NM_001100168.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:167550497 G>T maps to NM_004367.5 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:167550794 G>A maps to NM_004367.5 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:38711929 G>T maps to NM_001838.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr4:139966420 C>T maps to NM_012118.2 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr4:139966109 T>C maps to NM_012118.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr1:156287293 G>T maps to NM_005998.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:156288775 G>A maps to NM_005998.4 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:156280935 G>C maps to NM_005998.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:10250466 G>T maps to NM_012073.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:56127248 T>A maps to NM_001762.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:56130729 C>G maps to NM_001762.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:73476156 C>G maps to NM_006429.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:73466916 T>C maps to NM_006429.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:17073173 G>A maps to NM_014406.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:117561159 G>A maps to NM_004258.3 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:117561006 G>T maps to NM_004258.3 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr6:74477845 A>G maps to NM_133493.3 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr5:140012006 C>A maps to NM_001174105.1 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr12:7635987 C>T maps to NM_004244.4 K1021K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:7640015 A>G maps to NM_004244.4 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:7647931 C>A maps to NM_004244.4 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr12:7640564 G>A maps to NM_004244.4 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:7633837 C>A maps to NM_004244.4 E1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr12:7636216 C>T maps to NM_004244.4 W945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:7647889 C>A maps to NM_004244.4 G403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:7559320 G>A maps to ENST00000416109 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr12:7527188 C>T maps to ENST00000416109 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr12:7593777 C>T maps to ENST00000416109 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:27709154 T>A maps to NM_207397.2 K31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:43864423 G>T maps to NM_020406.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:66479328 G>A maps to NM_005582.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr16:28948960 C>T maps to NM_001178098.1 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr16:28944823 C>A maps to NM_001178098.1 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:28943341 C>A maps to NM_001178098.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr1:158225132 G>A maps to NM_001763.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:158226843 C>T maps to NM_001763.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:158300624 G>T maps to NM_001764.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:158263071 G>T maps to NM_001765.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr1:158151512 T>C did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:158151293 C>T maps to NM_001766.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:158326589 C>T maps to NM_030893.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:158325726 C>A maps to NM_030893.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:158326362 C>G maps to NM_030893.3 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:158324245 C>T maps to NM_030893.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:117297466 G>C maps to NM_001767.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:117297542 T>C maps to NM_001767.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:71060875 C>A maps to NM_015717.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr19:7812231 G>A maps to NM_021155.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:7810767 G>C maps to NM_021155.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr19:7812351 C>A maps to NM_021155.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:7812212 G>T maps to NM_021155.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr19:35822954 C>A maps to NM_001771.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:35823510 C>T maps to NM_001771.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr18:67563246 G>A maps to NM_006566.2 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:66082941 G>A maps to NM_020404.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:66083756 C>A maps to NM_020404.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:66082623 G>A maps to NM_020404.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:6560173 A>T maps to NM_001242.4 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr15:73996673 G>T maps to NM_001024736.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:204599595 C>T maps to NM_006139.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr17:72469885 C>G maps to NM_007261.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72541057 G>A maps to NM_006678.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr17:72539070 G>T maps to NM_006678.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:72539079 T>A maps to NM_006678.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72613440 C>T maps to ENST00000426295 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr17:72522133 T>A maps to NM_174892.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr17:72700779 C>T maps to ENST00000412086 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:41931262 C>A maps to NM_145273.3 Y190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:208084407 G>A maps to NM_001025109.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:208073313 A>T maps to NM_001025109.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr7:80290393 C>A maps to NM_001127444.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr19:49838975 C>A maps to NM_001774.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:6927602 C>T maps to NM_000616.4 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:6925469 C>T maps to NM_000616.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr20:44755306 C>T maps to NM_001250.4 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:135741237 C>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:135738537 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:135741405 C>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:35227748 C>G maps to NM_000610.3 S458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:60885659 G>A maps to NM_014207.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:60886820 C>A maps to NM_014207.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:111440441 G>A maps to NM_000560.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:111435127 C>A maps to NM_000560.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:117078705 G>C maps to NM_001779.2 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:117087218 G>A maps to NM_001779.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:157804344 G>A maps to NM_005894.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:157803065 C>A maps to NM_005894.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr1:157805708 C>A maps to NM_005894.2 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:60780937 G>A maps to NM_006725.3 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr12:56119958 A>G maps to NM_001780.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr12:9913368 C>A maps to NM_001781.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr9:35616042 C>A maps to NM_001782.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr17:62007147 G>T maps to NM_001039933.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:160523877 A>G maps to NM_001184879.1 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:160535365 G>C maps to NM_001184879.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr3:121825252 G>A maps to NM_175862.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:87085228 G>A maps to NM_172213.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:87085417 C>T maps to NM_172213.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:87085348 C>T maps to NM_172213.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:111296347 G>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:111298028 T>A maps to NM_198196.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr3:111325604 C>T maps to NM_198196.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:111319668 C>G maps to NM_198196.2 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:14518790 C>A maps to NM_078481.2 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr19:14517526 T>C maps to NM_078481.2 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:2637712 G>C did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:2640678 G>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:149999759 C>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:149963706 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:149937523 C>A did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr9:99296824 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:137542256 C>A maps to NM_004661.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr5:137524750 G>C maps to NM_004661.3 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:3781421 G>A maps to NM_021873.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:45219265 G>A maps to NM_001114091.1 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr17:45232091 G>A maps to NM_001114091.1 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:10506131 C>A maps to NM_007065.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr9:4685025 C>A maps to NM_017913.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr6:110538959 C>T maps to NM_015891.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:110540977 C>A maps to NM_015891.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr6:110540600 A>T maps to NM_015891.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:227300015 C>T maps to ENST00000366766 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:103412889 C>A maps to NM_006035.3 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:103416103 G>A maps to NM_006035.3 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr14:103410591 C>T maps to NM_006035.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:64606675 C>T maps to NM_017525.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr2:37873427 C>A maps to NM_006449.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr22:19502549 G>C maps to NM_001178010.1 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr22:19483536 A>G maps to NM_001178010.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:38449706 G>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:91989990 G>T maps to NM_001134420.1 *575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:193172941 G>T maps to NM_024529.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:193218962 T>C maps to NM_024529.4 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:193099324 A>T maps to NM_024529.4 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:25364167 T>C maps to ENST00000434814 Y663Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr7:21948029 G>A maps to NM_018719.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:38158661 G>T maps to NM_018101.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:45152241 G>A maps to NM_022842.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:45132935 C>A maps to NM_022842.3 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:45132779 G>A maps to NM_022842.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:54607065 G>A maps to NM_201546.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:24487842 G>A maps to NM_006727.3 R766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:24487999 G>A maps to NM_006727.3 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:24511540 C>T maps to NM_006727.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr5:24488076 G>T maps to NM_006727.3 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr5:24593421 G>A maps to NM_006727.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr5:24492941 T>A maps to NM_006727.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:24593446 A>G maps to NM_006727.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr5:24491936 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr5:24535932 T>C did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:24511480 G>T maps to NM_006727.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr5:24535923 A>G maps to NM_006727.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr5:24491928 A>T maps to NM_006727.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr5:24488151 C>A maps to NM_006727.3 G663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr5:24509760 C>A maps to NM_006727.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:65016126 G>A maps to NM_001797.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:65022191 T>C maps to NM_001797.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr16:65022114 G>T maps to NM_001797.2 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr16:65016006 G>A maps to NM_001797.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr5:22078736 C>A maps to NM_004061.3 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr5:21854840 A>G maps to NM_004061.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:21752082 G>A maps to NM_004061.3 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr5:21842268 C>T did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr5:22078743 C>A maps to NM_004061.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:21854885 G>A maps to NM_004061.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:21975298 C>A maps to NM_004061.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr5:21842273 G>C maps to NM_004061.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr5:21842438 T>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:21975444 G>C maps to NM_004061.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:21975464 G>A maps to NM_004061.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:21755940 C>T maps to NM_004061.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:21760769 G>T maps to NM_004061.3 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:22078647 C>A maps to NM_004061.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:66950227 C>A maps to NM_004062.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr16:66949989 C>T maps to NM_004062.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr16:66944337 G>T maps to NM_004062.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr8:95164229 C>A maps to NM_001144663.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr8:95186468 G>A maps to NM_001144663.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:19473547 C>A maps to NM_004934.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr5:19483467 C>T maps to NM_004934.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr5:19520840 C>A maps to NM_004934.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:19483488 A>G maps to NM_004934.3 H601H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr5:19544050 G>T maps to NM_004934.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr5:19747336 G>T maps to NM_004934.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:19721510 C>A maps to NM_004934.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:19473457 G>A maps to NM_004934.3 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:19544110 G>C maps to NM_004934.3 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:19483468 G>T maps to NM_004934.3 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:64211221 C>T maps to NM_021153.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr18:64235677 G>T maps to NM_021153.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr18:64197171 C>T maps to NM_021153.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr18:25585834 T>A maps to NM_001792.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr18:59166690 T>A maps to NM_031891.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr20:44806639 G>A maps to NM_021248.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr20:44869815 G>T maps to NM_021248.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr10:73574710 G>C maps to ENST00000398860 L3252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr10:73558234 G>A maps to ENST00000398860 V2323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr10:73560460 C>A maps to ENST00000398860 A2482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:73464783 C>A maps to ENST00000398860 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr10:73326641 G>T maps to ENST00000398860 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr10:73406253 T>C maps to ENST00000398860 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:73461825 C>A maps to ENST00000398860 Y820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr20:58545156 A>T maps to NM_177980.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:60504841 G>A maps to NM_001794.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:60427940 G>A maps to NM_001794.2 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr16:66434917 A>T maps to NM_001795.3 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr16:66430102 T>A maps to NM_001795.3 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr5:31299679 C>A maps to NM_004932.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr5:31323237 C>T maps to NM_004932.2 Y732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr5:31299569 G>T did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:31317837 C>A maps to NM_004932.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:63511244 G>A maps to NM_004361.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:63547736 C>T maps to NM_004361.2 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:63489422 A>T maps to NM_004361.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr18:63491902 G>T maps to NM_004361.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr16:61761072 C>T maps to NM_001796.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr16:61747769 C>T maps to NM_001796.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr16:61854865 A>G maps to NM_001796.2 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:61891021 C>G did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr16:61854937 A>T maps to NM_001796.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr16:62055226 A>T maps to NM_001796.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:26886135 G>A maps to NM_016279.3 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:26915831 C>T maps to NM_016279.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:26988257 G>A maps to NM_016279.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr5:26886150 G>T maps to NM_016279.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:26881477 G>A maps to NM_016279.3 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:26915836 C>A maps to NM_016279.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:26916020 G>A maps to NM_016279.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr5:26881655 C>A maps to NM_016279.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr5:26902712 T>C maps to NM_016279.3 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:26885765 C>A maps to NM_016279.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:26916005 A>G maps to NM_016279.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr5:26890630 A>G maps to NM_016279.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:85968082 C>T maps to NM_033100.2 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:85971450 C>A maps to NM_033100.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr10:85973842 C>G maps to NM_033100.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:85968558 G>C maps to NM_033100.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:176016138 G>A maps to NM_001171976.1 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr5:176003182 C>T maps to NM_001171976.1 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:176011259 G>T maps to NM_001171976.1 G710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:105658487 C>T maps to NM_152750.4 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr11:618688 G>A maps to NM_021924.4 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:89756977 C>T maps to NM_052988.4 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr16:89761138 C>A maps to NM_052988.4 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:1636453 C>A maps to NM_024011.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:1635742 C>T maps to NM_024011.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:37687304 C>T maps to NM_016507.2 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:37687205 G>T maps to NM_016507.2 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr17:37672055 G>A maps to NM_016507.2 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr17:37627539 G>A maps to NM_016507.2 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr7:40134110 C>T maps to NM_003718.4 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:90613555 G>T maps to NM_012395.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr7:90419917 G>A maps to NM_012395.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:90419887 G>A maps to NM_012395.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr23:47086598 G>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:96691045 A>T did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:96683065 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:205499822 C>T maps to NM_212503.2 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:205496950 C>T maps to NM_212503.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:110944070 C>A maps to NM_015076.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:110953346 T>A maps to NM_015076.3 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr6:110935788 C>A maps to NM_015076.3 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr9:90584107 C>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr17:73998414 C>T maps to NM_001258.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr17:73998596 G>A maps to NM_001258.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:30815060 G>T maps to NM_003885.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr20:31967386 G>T maps to ENST00000357886 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr20:31967305 G>T maps to ENST00000357886 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr9:123330664 C>T maps to NM_018249.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:26974587 A>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:26971322 A>G maps to NM_001260.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:21201498 G>A maps to NM_017774.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr14:50799105 C>T maps to NM_004196.3 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:76523341 T>C maps to ENST00000307465 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr5:133644402 C>T maps to NM_001113575.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:18631344 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:18622326 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:18616695 A>C did not map to a codon.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:21971002 C>A maps to NM_001195132.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr9:21974791 G>T maps to NM_001195132.1 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr9:21971081 G>A maps to NM_001195132.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-60-2725-01A-01D-1267-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr9:21974747 C>A maps to NM_001195132.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:184367325 C>A maps to NM_017632.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:125880415 G>A maps to ENST00000392693 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:139866288 A>G did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:139866313 A>G did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:139866205 G>A did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:139865875 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:139866046 C>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr17:15516030 C>T maps to ENST00000455584 W693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr17:14139247 G>C maps to NM_001007530.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr4:85530641 G>A maps to NM_001263.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr20:5157334 T>A maps to NM_003818.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:31083909 G>T maps to NM_001264.4 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:88870963 C>T maps to NM_030928.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr13:28539153 T>C did not map to a codon.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:72673419 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:72667452 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:72674403 G>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:45211184 C>A maps to ENST00000396750 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:45207357 T>A maps to ENST00000396750 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:51981925 G>T maps to NM_001080405.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr19:51984758 T>C maps to NM_001080405.1 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr19:45179576 C>T maps to NM_020219.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:45024763 G>A maps to NM_001102597.1 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr19:45017313 G>A maps to NM_001102597.1 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:42085841 G>A maps to NM_001098506.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr19:42083651 G>A maps to NM_001098506.1 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:42219049 T>C maps to NM_004363.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr19:42219743 T>C maps to NM_004363.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:42187818 G>A maps to NM_006890.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:42191132 C>T maps to NM_006890.3 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:33792244 C>G maps to NM_004364.3 *359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr20:48808475 G>A maps to NM_005194.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:33870399 G>A maps to NM_001806.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:37455704 T>A maps to NM_005760.2 K211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr22:17690369 G>C maps to NM_017424.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr22:18022265 C>T maps to ENST00000400579 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:18022048 G>A maps to ENST00000400579 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr22:18022204 G>A maps to ENST00000400579 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:17619153 C>A maps to NM_033070.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:17619129 T>A maps to NM_033070.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:135942041 C>T maps to NM_001807.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr9:135941992 C>T maps to NM_001807.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:15788057 C>G maps to ENST00000375924 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:22336259 G>T maps to NM_005747.4 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:22307650 G>C maps to NM_007352.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:11259436 G>A maps to NM_006561.3 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr18:34901832 C>A maps to NM_020180.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr18:34839188 G>A maps to NM_020180.3 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr18:34850746 G>A maps to NM_020180.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:3282473 C>A maps to NM_021938.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr19:3278101 C>T maps to NM_021938.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr19:3293413 G>A maps to NM_021938.3 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr15:72582590 G>A maps to NM_052840.4 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr22:46760591 G>A maps to NM_014246.1 Q2866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr22:46859694 G>A maps to NM_014246.1 I1364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr22:46780530 C>A maps to NM_014246.1 P2264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:109815821 A>T maps to NM_001408.2 P2791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:109812420 C>G maps to NM_001408.2 L2362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr1:109806323 C>G maps to NM_001408.2 L1642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:109803811 G>T maps to NM_001408.2 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:48692592 C>T maps to NM_001407.2 K1624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr3:48698816 C>T maps to NM_001407.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:48678784 A>G maps to NM_001407.2 S2999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:48677680 C>A maps to NM_001407.2 E3113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:48682911 G>A maps to NM_001407.2 L2587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:48682971 G>C maps to NM_001407.2 L2567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:3766826 C>A maps to NM_001810.5 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr4:68380251 T>C maps to NM_001812.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr4:104067179 C>A maps to NM_001813.2 E1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:104032073 C>T maps to NM_001813.2 L2545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr4:104068578 C>A maps to NM_001813.2 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:104054853 C>A maps to NM_001813.2 E2240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:214805945 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:214816280 G>T maps to NM_016343.3 E1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:214787148 C>T maps to NM_016343.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:100387223 C>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:100382612 C>G did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:100364556 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:100417909 C>G did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:100402955 A>T did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr5:64850710 C>A maps to NM_022145.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:95099821 G>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr9:123875856 A>T maps to NM_007018.4 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr9:123908434 A>T maps to NM_007018.4 R1120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr9:123903706 G>A maps to NM_007018.4 Q844Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr4:56875951 G>C maps to NM_025009.3 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr4:56820421 T>A maps to NM_025009.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr4:56831871 C>T maps to NM_025009.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:49048573 C>G maps to NM_001194998.1 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr15:49081012 G>C maps to NM_001194998.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:117280364 G>A maps to NM_014956.4 K1260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:117265652 T>C maps to NM_014956.4 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr11:117244506 C>G maps to NM_014956.4 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr11:117244537 C>T maps to NM_014956.4 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:243328006 T>C maps to NM_014812.2 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr18:13048934 C>T maps to NM_032142.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr18:13056423 C>T maps to NM_032142.3 Q1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr18:13073109 C>A maps to NM_032142.3 R1848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr20:34099247 C>T maps to NM_007186.3 I2374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:88484528 G>C maps to NM_025114.3 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:88479930 G>C maps to NM_025114.3 S1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:179989081 A>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:179993628 C>T maps to NM_014810.4 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:179965808 G>T maps to NM_014810.4 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:179966092 C>A maps to NM_014810.4 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:180062649 C>T maps to NM_014810.4 R2470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:179983507 T>C maps to NM_014810.4 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:180003167 G>A maps to NM_014810.4 L1299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:95546719 C>T maps to NM_014679.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:134277096 G>T maps to NM_025180.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:134270793 C>A maps to NM_025180.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:138291715 G>T maps to NM_024491.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr5:635484 A>G did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:637809 C>T maps to NM_018140.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr9:80879232 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:80856684 G>A maps to NM_001098802.1 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr9:14720183 C>A maps to NM_005454.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr22:47089396 G>T maps to NM_022766.5 C351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr22:47089353 T>A maps to NM_022766.5 K366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr22:47108145 C>A maps to NM_022766.5 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr22:47095312 G>T maps to NM_022766.5 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr16:55844886 C>A maps to NM_001025195.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr16:66977822 G>T maps to NM_003869.5 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr16:66977218 G>T maps to NM_003869.5 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:55886868 G>A maps to NM_001143685.1 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr16:55880744 G>A maps to NM_001143685.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:89703554 A>G maps to NM_004365.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:31918166 C>A maps to ENST00000437789 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr6:31914820 G>T maps to ENST00000437789 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:131356250 C>A maps to NM_032545.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:196642291 G>A maps to NM_000186.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:196920099 G>A maps to ENST00000367421 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:196748445 T>C maps to NM_021023.5 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:196887530 G>T maps to NM_006684.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:196882044 T>A maps to NM_006684.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:196871617 C>A maps to NM_006684.2 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:196952177 A>G maps to ENST00000367414 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:196946814 A>T maps to ENST00000367414 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:196965149 A>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:196953256 C>T maps to ENST00000367414 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr1:196965331 G>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:35182473 T>C maps to NM_138638.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:202005137 C>T maps to NM_001127183.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr23:47486232 G>T did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr7:117232170 C>T maps to NM_000492.3 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:117149086 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:49557572 G>C maps to ENST00000377280 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr1:151491774 C>A maps to NM_020770.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:57730259 C>A maps to NM_032866.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:27327224 A>G maps to ENST00000404694 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr14:54989296 C>G maps to NM_006568.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:55004941 G>T maps to NM_006568.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr2:54001451 T>C maps to NM_001008708.2 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:48545631 G>A maps to NM_001267.2 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr21:37763858 C>A maps to NM_005441.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr21:37775111 G>T maps to NM_005441.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:50824632 C>T maps to NM_020549.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr10:50870713 C>T maps to NM_020549.4 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:50856550 A>G did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:50835661 C>G maps to NM_020549.4 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:56172044 C>T maps to NM_016139.2 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:146757104 G>A maps to NM_004284.3 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr1:146739122 C>T maps to NM_004284.3 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:146765332 C>G maps to NM_004284.3 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:93467574 G>T maps to NM_001271.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:93480846 C>A maps to NM_001271.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr15:93498729 C>G maps to NM_001271.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr17:7798754 A>T maps to NM_001005271.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:7806031 C>A maps to NM_001005271.2 I1178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr12:6707130 C>T maps to ENST00000309577 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:6212537 C>T maps to NM_015557.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr1:6185835 C>T maps to NM_015557.2 P1387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:6196586 C>A maps to NM_015557.2 E896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:6196611 G>A maps to NM_015557.2 F887F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:40052231 G>A maps to NM_032221.3 S1485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:40080607 C>T maps to NM_032221.3 E1127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr20:40043903 C>A maps to NM_032221.3 R2287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr20:40050342 T>C maps to NM_032221.3 T1644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:40102042 C>A maps to NM_032221.3 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:40045304 G>A maps to NM_032221.3 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr8:61736457 T>A maps to NM_017780.2 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr8:61749417 C>A maps to NM_017780.2 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr8:61707580 G>A maps to NM_017780.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr8:61765995 G>T maps to NM_017780.2 E2238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:61757512 G>C maps to NM_017780.2 L1647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:61754597 C>T maps to NM_017780.2 L1613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:61749489 A>T maps to NM_017780.2 A1368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:61774819 C>T maps to NM_017780.2 N2632N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr8:61655235 G>A maps to NM_017780.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:61750801 C>T maps to NM_017780.2 S1507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr14:21859632 G>A maps to NM_001170629.1 R2352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:21884066 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:53338388 C>T maps to ENST00000219084 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:53358336 A>T maps to ENST00000219084 K2742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr16:53338367 C>T maps to ENST00000219084 S2150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:53852088 G>A maps to NM_018397.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:125513736 G>T maps to NM_001274.4 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr12:133419613 C>T maps to NM_001161344.1 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr20:5903528 G>T maps to NM_001819.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:5903357 G>T maps to NM_001819.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr20:5903668 C>T maps to NM_001819.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr20:5905691 C>G maps to NM_001819.2 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:111777526 A>G did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:111855004 G>A maps to NM_201653.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:111857927 G>A maps to NM_201653.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:111861203 G>C maps to NM_201653.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:884147 G>A maps to NM_001142676.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:203192297 A>G maps to NM_003465.2 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:203188957 C>T maps to NM_003465.2 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:203186085 C>G maps to NM_003465.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr22:51019076 C>T maps to NM_005198.4 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr3:361467 G>T maps to NM_006614.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:85156111 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:85302528 T>G did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:85218963 A>G did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:85218783 C>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr20:32438838 G>A maps to NM_176812.4 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:78969518 G>A maps to NM_024591.4 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr17:78972931 G>T maps to NM_024591.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:23114091 C>A maps to NM_152272.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:19629006 G>T maps to NM_024944.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr21:19629099 C>A maps to NM_024944.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr21:19635168 G>A maps to NM_024944.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:89939368 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:41555037 G>A maps to NM_007236.4 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr16:23768852 C>G maps to NM_022097.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:220406628 A>C maps to NM_024536.5 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr2:220404599 G>A maps to NM_024536.5 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr2:220405115 C>T maps to NM_024536.5 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:220404185 G>A maps to NM_024536.5 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr3:184104630 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:109931895 T>C did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:109963155 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:109963157 T>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:109937484 C>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:109924817 G>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:74414012 C>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:74413876 G>T maps to NM_015424.3 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:136700850 T>C maps to NM_001006628.1 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr7:136700604 C>G maps to NM_001006628.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr7:136700520 G>A maps to NM_001006628.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr7:136700697 C>A maps to NM_001006628.1 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr7:136700019 C>A maps to NM_001006628.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:240071954 G>T maps to NM_000740.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:240072469 C>G maps to NM_000740.2 Y573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:46406688 C>T maps to NM_000741.2 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:46407306 C>G maps to NM_000741.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:46408055 G>A maps to NM_000741.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr2:175618375 G>A maps to NM_001039523.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr2:175618288 G>T maps to NM_001039523.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:3691058 G>A maps to NM_020402.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:61981025 C>T maps to NM_000744.5 K579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr20:61982048 G>A maps to NM_000744.5 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:42623537 C>A maps to NM_004198.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr8:42608375 A>G maps to NM_004198.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr8:42611339 C>A maps to NM_004198.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr8:42611900 G>T maps to NM_004198.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:154542076 C>T maps to NM_000748.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr8:42587226 G>A maps to NM_000749.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:78921716 G>A maps to NM_000750.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:233390966 G>A maps to NM_000751.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:233393324 C>G maps to NM_000751.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:4805915 C>T maps to NM_000080.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:233404756 C>A maps to NM_005199.4 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:233410279 C>A maps to NM_005199.4 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:233409213 C>G maps to NM_005199.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:233410279 C>A maps to NM_005199.4 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:45672149 C>T maps to NM_003654.4 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr11:45671651 C>A maps to NM_003654.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:105150890 G>T maps to NM_018413.5 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:2472882 G>A maps to NM_018641.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr10:73767079 C>A maps to NM_004273.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr10:73765714 G>T maps to NM_004273.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr19:34263301 C>A maps to NM_022467.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:69154501 G>A maps to NM_001039690.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:101964283 C>A maps to NM_001278.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:78403566 G>T maps to NM_006383.2 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:16280443 C>G maps to NM_054113.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:26864146 C>T maps to NM_001029881.1 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr18:12274249 C>T maps to ENST00000342845 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr18:12277259 G>T maps to ENST00000342845 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr16:11009504 G>T maps to NM_000246.3 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr16:10996608 G>A maps to NM_000246.3 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr15:65499326 G>T maps to NM_003613.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:65489731 C>T maps to NM_003613.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr15:65490997 C>A maps to NM_003613.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:19654547 G>A maps to NM_153221.2 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr19:19655798 C>T maps to NM_153221.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr19:19656164 G>T maps to NM_153221.2 R937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr14:102816310 A>G maps to NM_001177611.1 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:1271622 C>A maps to ENST00000413636 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr4:103790339 C>G maps to NM_001008388.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:120135580 G>C maps to ENST00000392521 S1922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:120139706 G>A maps to ENST00000392521 L1787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr9:130931779 G>A maps to NM_012127.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:113498468 C>G maps to NM_152515.3 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:113509923 C>A maps to NM_152515.3 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr11:46782307 G>A maps to ENST00000415402 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:45822919 C>A maps to NM_001824.3 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:43990940 T>C maps to ENST00000424065 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:80554959 C>T maps to NM_001825.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr5:80548573 C>A maps to NM_001825.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:80559432 G>T maps to NM_001825.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:122285373 C>G did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr2:122227507 C>T maps to NM_015282.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr3:33617710 G>A maps to ENST00000359576 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:86919104 C>A maps to NM_006536.5 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:86907181 A>T maps to NM_006536.5 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:87031643 T>C maps to ENST00000263723 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:87025690 T>G maps to ENST00000263723 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:87031603 C>A maps to ENST00000263723 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:143048730 C>T maps to NM_000083.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr7:143043684 C>G maps to NM_000083.2 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:184071920 G>A maps to NM_004366.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr3:184074815 C>G maps to NM_004366.4 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:184075156 C>A maps to NM_004366.4 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:10163114 G>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:10176329 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:10182001 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:49851291 C>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:49855382 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:49854834 G>C did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:49840469 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:11887199 C>T maps to ENST00000376496 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:1501633 G>A maps to ENST00000382745 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr16:1499071 C>T maps to ENST00000382745 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:16358207 C>A maps to NM_004070.3 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr3:190026065 T>G maps to NM_021101.4 *212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:190039818 G>A maps to NM_021101.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr13:96086269 C>T maps to NM_182848.3 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:90042514 G>T maps to NM_001185072.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:190126223 C>A maps to NM_006580.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:190122606 G>T maps to NM_006580.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr21:31538287 A>T maps to NM_012131.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:106171780 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:155597294 C>T maps to NM_001001346.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:184241241 C>A maps to NM_001111319.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr22:19511187 G>T maps to NM_003277.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:10133280 C>A maps to ENST00000355690 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr12:10167164 G>A maps to NM_001129998.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr14:38724624 G>T maps to NM_175060.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr14:38724714 G>A maps to NM_175060.1 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr14:38724723 G>A maps to NM_175060.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:11066807 C>A maps to ENST00000409790 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:11145374 G>A maps to ENST00000409790 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr16:11217768 C>T maps to ENST00000409790 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr16:11056371 C>T maps to ENST00000409790 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr16:70219865 C>T maps to NM_173619.2 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:78062079 G>T maps to NM_005752.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:8281902 A>G maps to NM_016184.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr12:8290777 C>T maps to NM_016184.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:7894076 G>A maps to NM_130441.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr12:8692490 G>A maps to NM_014358.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:71046961 G>A maps to NM_173535.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr2:71036441 G>A maps to NM_173535.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:7831058 C>T maps to NM_014257.4 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr19:7831638 C>G maps to NM_014257.4 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:8629925 C>T maps to NM_001007033.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr12:9885653 C>T maps to NM_172004.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr12:9885650 G>A maps to NM_172004.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr4:141320054 C>T maps to NM_004362.2 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:45917078 G>A maps to NM_001114086.1 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr21:36079603 A>T maps to ENST00000360731 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:122803816 C>A maps to ENST00000302528 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr7:73803541 C>T maps to NM_003388.4 A891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr7:73774518 C>T maps to NM_003388.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:73803458 G>T maps to NM_003388.4 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:29404719 G>T maps to ENST00000379543 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:155240699 C>G maps to ENST00000368361 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr8:1719294 C>T maps to NM_018941.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr8:1728420 C>G maps to NM_018941.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr4:10509581 C>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr4:56310046 G>C maps to NM_004898.2 S570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:57428586 C>A maps to NM_006831.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:35764999 C>T maps to NM_001832.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr19:45477733 A>G maps to NM_001294.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr19:45490528 G>T maps to NM_001294.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr5:1323905 T>A maps to NM_030782.3 K426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:1344485 A>G maps to NM_030782.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr5:1339042 G>A maps to NM_030782.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:65458971 C>T maps to NM_006660.3 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr3:150659450 G>T maps to NM_001195794.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:36205072 G>A maps to NM_022111.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:36203670 C>A maps to NM_022111.3 E1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:9791885 C>A maps to NM_001009566.1 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:9794027 A>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:9791326 G>A maps to NM_001009566.1 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:9811555 G>A maps to NM_001009566.1 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:9791431 C>A maps to NM_001009566.1 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:140281692 C>T maps to NM_022131.2 H751H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:140282881 G>T maps to NM_022131.2 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:140281054 T>A maps to NM_022131.2 L706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr3:140285002 G>T maps to NM_022131.2 E926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr3:140285065 G>T maps to NM_022131.2 E947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr3:139894791 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:140122640 G>T maps to NM_022131.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:57743956 A>G maps to NM_004859.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:57762523 C>A maps to NM_004859.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr22:19222103 C>G maps to NM_007098.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr22:19203622 G>A maps to NM_007098.3 H1021H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr8:27468013 C>A maps to NM_001831.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr16:3576428 C>T maps to NM_015041.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:627254 C>G maps to NM_199167.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:627164 C>A maps to NM_199167.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr8:62366773 C>T maps to NM_173519.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr8:62212823 C>G maps to NM_173519.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr8:62212664 C>A maps to NM_173519.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:123332128 G>T did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:123319197 C>A maps to NM_001010852.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:123384861 A>T maps to NM_001010852.2 K314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:100515264 C>T maps to NM_206808.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr13:100543576 C>A maps to NM_206808.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr13:100518605 A>T maps to NM_206808.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr12:22218071 G>T maps to NM_018686.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:10286598 A>G maps to NM_138809.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:81735266 C>T maps to NM_198390.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:7003613 G>A maps to NM_207315.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:7003643 G>A maps to NM_207315.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:7001357 C>A maps to NM_207315.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr16:66620910 C>T maps to NM_144673.2 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:66643808 C>A maps to NM_181553.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:23847658 C>T maps to ENST00000339180 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr5:79032598 G>T maps to NM_153610.3 E2671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr5:79028280 A>T maps to NM_153610.3 P1231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:79026606 A>C maps to NM_153610.3 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:79029969 A>T maps to NM_153610.3 T1794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:79031917 G>T maps to NM_153610.3 E2444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr5:79033023 G>C maps to NM_153610.3 L2812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr8:87917411 G>T maps to NM_173538.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr8:88365861 A>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr3:128890382 T>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr18:72245451 G>T maps to NM_032649.5 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:47939826 C>G maps to NM_001142564.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr4:47939382 G>A maps to NM_001142564.1 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:150911760 G>T did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr23:150911981 C>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:150911816 A>G did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:150911632 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:150908072 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:150909320 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:150911902 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:150912079 G>T did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:150912663 C>A did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:150912442 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:150911688 G>C did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr2:99013207 C>A maps to NM_001298.2 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:99013000 G>C maps to NM_001298.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:6262864 T>A maps to NM_001037329.2 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr11:6265536 C>T maps to NM_001037329.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr11:6261347 C>T maps to NM_001037329.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:58001178 C>T maps to NM_001297.4 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr16:57931764 C>T maps to NM_001297.4 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:87591015 C>T maps to NM_019098.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:87660079 G>T maps to NM_019098.4 C313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:87755765 G>C maps to NM_019098.4 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:87680337 G>A maps to NM_019098.4 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:87679236 C>T maps to NM_019098.4 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:21549973 G>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:21508630 C>G did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr23:21670576 G>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:21627563 A>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:21608736 A>C did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:21450922 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:21627349 G>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:21534641 G>C did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:21519701 C>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:21549998 G>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:21627281 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:21545096 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:21609253 G>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:21609199 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:1036485 C>G maps to NM_004368.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:95368959 C>A maps to NM_001839.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:104678749 C>T maps to NM_017649.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr2:97464818 G>A maps to NM_020184.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:97427869 C>A maps to NM_020184.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr12:70740016 A>G maps to NM_014515.5 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr19:54656310 G>T maps to NM_014516.3 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr7:135078942 C>A maps to NM_001190850.1 G452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:135073609 G>T maps to NM_001190848.1 S555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr7:135099077 A>C did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:135078670 T>A maps to NM_001190850.1 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:180001040 C>A maps to NM_015455.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr5:179996223 C>G maps to NM_015455.3 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:78647415 C>A maps to ENST00000512485 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr7:155301726 G>A maps to NM_001103176.1 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:88854624 G>T maps to NM_016083.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr6:88854318 C>T maps to NM_016083.4 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:88853832 C>T maps to NM_016083.4 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:24201816 G>A maps to NM_001841.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:24201726 G>A maps to NM_001841.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:246829020 C>T maps to NM_152609.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:246811035 T>C maps to NM_152609.2 C511C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:246797277 G>A maps to NM_152609.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:40955683 G>T maps to NM_173478.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:17487025 G>T maps to NM_017738.2 E1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr9:17409419 A>G maps to NM_017738.2 Q915Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:41337878 T>C maps to NM_001843.2 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:41327335 G>C maps to NM_001843.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:205039001 G>A maps to NM_005076.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:205033819 C>G maps to NM_005076.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:205033504 C>A maps to NM_005076.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:205033471 G>T maps to NM_005076.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:205039103 G>T maps to NM_005076.3 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr3:74334633 G>A maps to NM_020872.1 Y842Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr3:74313617 C>T maps to NM_020872.1 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:74414821 A>G maps to NM_020872.1 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:74411135 C>A maps to NM_020872.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:74385766 C>G maps to NM_020872.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:74413748 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:2908550 G>A maps to NM_175607.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr3:2787298 C>A maps to NM_175607.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:3095513 A>G maps to NM_175607.1 Q945Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr3:2787352 T>C maps to NM_175607.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:3030127 T>C maps to NM_175607.1 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:100141927 G>T maps to NM_014361.2 G757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr11:100211381 G>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:99944897 G>T maps to NM_014361.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:99944960 C>T maps to NM_014361.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:1363342 C>T maps to NM_014461.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:1262452 C>A maps to NM_014461.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr3:1269555 G>A maps to NM_014461.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:1262455 C>A maps to NM_014461.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr17:40842121 C>A maps to NM_003632.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr17:40845546 C>A maps to NM_003632.2 C995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:40843899 G>T maps to NM_003632.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:146536823 C>G maps to NM_014141.5 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:146818116 A>G maps to NM_014141.5 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:147600753 C>A maps to NM_014141.5 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr7:148112555 C>T maps to NM_014141.5 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr7:146741039 C>T maps to NM_014141.5 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:147914554 C>T maps to NM_014141.5 C1062C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:146805422 G>A maps to NM_014141.5 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr7:147815228 C>A maps to NM_014141.5 A801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr7:146825876 C>A maps to NM_014141.5 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr7:146829518 G>T maps to NM_014141.5 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr7:146805263 C>A maps to NM_014141.5 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr7:147336264 A>T maps to NM_014141.5 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:147926792 C>T maps to NM_014141.5 D1101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:147815243 A>T maps to NM_014141.5 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:147259237 G>T maps to NM_014141.5 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:39086790 G>T maps to NM_033655.3 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:76523670 C>T maps to NM_033401.3 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr16:76573653 G>T maps to NM_033401.3 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr16:76501304 G>T maps to NM_033401.3 G513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr16:76461468 C>T maps to NM_033401.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:125175153 C>A maps to NM_130773.2 Y172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:125627271 C>T maps to NM_130773.2 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr2:125284886 C>A maps to NM_130773.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:125530502 C>A maps to NM_130773.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:125669110 C>T maps to NM_130773.2 I1240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:125555883 G>T maps to NM_130773.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr2:125204396 G>A maps to NM_130773.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:125521620 G>T maps to NM_130773.2 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:125261957 C>A maps to NM_130773.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:125547542 G>A maps to NM_130773.2 Q938Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr2:125262046 C>A maps to NM_130773.2 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:125261960 C>A maps to NM_130773.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:125261972 G>A maps to NM_130773.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr17:7840480 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:40714915 C>T maps to NM_001042532.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr17:40717011 A>T maps to NM_001042532.2 K446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr17:40717708 C>T maps to NM_001042532.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr7:51096397 G>A maps to ENST00000395542 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr7:51111273 G>A maps to ENST00000395542 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:165542494 G>C maps to ENST00000392717 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:31354660 G>C maps to NM_004086.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:31355339 C>T maps to NM_004086.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:230795271 G>A maps to NM_007357.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr1:230827304 G>T maps to NM_007357.2 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:70531125 G>A maps to NM_015386.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr7:107002555 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr7:106938786 C>T maps to NM_006348.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr13:40261702 G>A maps to ENST00000255468 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr13:40233517 C>G maps to ENST00000255468 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr16:23446016 C>T maps to NM_153603.3 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:55027747 A>T maps to NM_004645.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:116441970 A>G maps to NM_000493.3 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:103470045 T>C did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:103471653 T>C maps to NM_080629.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:103488509 C>A maps to NM_080629.2 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:103444261 A>G did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:103364269 A>C maps to NM_080629.2 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:103453202 G>A maps to NM_080629.2 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:103428315 C>A maps to NM_080629.2 G985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:103412502 C>A maps to NM_080629.2 G1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:103404589 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:103380301 A>T maps to NM_080629.2 G1306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr1:103491774 C>T maps to NM_001854.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:103481244 A>T maps to NM_080629.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:103480072 C>T maps to NM_080629.2 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:103444939 G>T maps to NM_080629.2 R882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:103355027 C>A maps to NM_080629.2 G1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:33132202 G>A maps to NM_080680.2 L1637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:33147524 G>A maps to NM_080680.2 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr6:75893693 C>T maps to ENST00000322507 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr6:75892985 G>A maps to ENST00000322507 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:75848582 G>C maps to ENST00000322507 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr6:75831143 G>T maps to ENST00000322507 A2320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:75833799 T>C maps to ENST00000322507 G2245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:75887481 T>C maps to ENST00000322507 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:75893639 G>A maps to ENST00000322507 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:75825591 A>T maps to ENST00000322507 A2535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:121243857 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:121322261 C>T maps to NM_021110.1 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr8:121259858 C>A maps to NM_021110.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:101806875 C>T maps to NM_001855.3 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr9:101778304 C>G maps to NM_001855.3 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:101747922 A>T maps to NM_001855.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:101829240 T>A maps to NM_001855.3 A1243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:101751483 C>T maps to NM_001855.3 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:32154545 C>A maps to NM_001856.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr1:32148970 C>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr1:32167758 G>A maps to NM_001856.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr10:105830202 C>G maps to NM_000494.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:105796277 C>G maps to NM_000494.3 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:105824223 G>A maps to NM_000494.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:105814741 T>A maps to NM_000494.3 K581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr21:46896338 G>T maps to ENST00000359759 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr21:46925828 C>T maps to ENST00000359759 A1470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr21:46932275 C>G maps to ENST00000359759 L1743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr6:70812095 A>G maps to NM_001858.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr6:70637828 G>T maps to NM_001858.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr6:70610161 A>G maps to NM_001858.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr6:70778329 C>T maps to NM_001858.4 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:70866578 G>T maps to NM_001858.4 R752R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:70859618 G>A maps to NM_001858.4 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:70894800 A>G maps to NM_001858.4 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:48270366 G>A maps to NM_000088.3 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:48266582 G>A maps to NM_000088.3 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr17:48266735 A>G did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:94038086 C>T maps to NM_000089.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:94038907 C>T maps to NM_000089.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr7:94049585 T>A maps to NM_000089.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:94059647 C>T maps to NM_000089.3 D1348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:94058502 G>T maps to NM_000089.3 E1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:94035031 C>A maps to NM_000089.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr20:61936823 G>T maps to ENST00000326996 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:61959480 T>A maps to ENST00000326996 C1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr6:55922601 T>A maps to NM_030820.3 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:139611077 C>A maps to NM_152888.1 G1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:139838948 C>T maps to NM_152888.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:139614403 T>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:139696706 G>C maps to NM_152888.1 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:139601597 A>T maps to NM_152888.1 P1593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:139629156 C>T maps to NM_152888.1 R1290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr8:139838951 C>T maps to NM_152888.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr8:139706803 C>A maps to NM_152888.1 G883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:86437075 C>A maps to NM_152890.5 G789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:86203189 T>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr1:86252090 T>C maps to NM_152890.5 P1335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:86523648 C>A maps to NM_152890.5 G606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:86591139 G>A maps to NM_152890.5 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr4:109895697 T>C maps to ENST00000333642 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:110221758 G>T maps to ENST00000333642 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr4:109767294 C>T maps to ENST00000333642 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:117064381 C>T maps to NM_032888.2 I1622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:116984502 G>T maps to NM_032888.2 G808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr9:117051247 G>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:116925042 C>G maps to NM_032888.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:7484114 C>T maps to NM_001037763.2 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:7472139 C>T maps to NM_001037763.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:7571509 G>A maps to NM_001037763.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:7410439 T>C maps to NM_001037763.2 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr7:7476073 C>T maps to NM_001037763.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:7572455 C>A maps to NM_001037763.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr12:48380865 G>A maps to NM_001844.4 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:48378343 A>T maps to NM_001844.4 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr12:48380193 G>A maps to NM_001844.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:48387258 G>A maps to NM_001844.4 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:189861889 G>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr2:189855087 T>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:110826823 C>T maps to NM_001845.4 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr13:110818650 C>G did not map to a codon.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr13:110864802 C>T maps to NM_001845.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr13:110853788 T>A maps to NM_001845.4 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr13:111117774 A>G maps to NM_001846.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr13:111098174 G>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr13:111155573 C>T maps to NM_001846.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr13:111143634 G>C maps to NM_001846.2 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:228172618 C>T maps to NM_000091.4 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:228175575 C>T maps to NM_000091.4 L1614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:228135632 G>T maps to NM_000091.4 G575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:228137729 A>T maps to NM_000091.4 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:228148490 G>T maps to NM_000091.4 G889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:227895294 G>T maps to ENST00000396625 G1279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:227917018 A>T did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr2:227924178 A>G maps to ENST00000396625 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr2:227924169 C>A maps to ENST00000396625 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:107840242 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:107869497 C>T did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr23:107834431 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:107408617 C>T did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:107446159 G>T did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:107402737 C>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:107431173 T>C did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:107404947 C>A did not map to a codon.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr23:107449747 T>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:107403858 G>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr9:137714872 C>A maps to NM_000093.3 G1546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr9:137677894 G>C did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr9:137642655 C>A maps to NM_000093.3 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:137642703 G>A maps to NM_000093.3 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr9:137717707 C>T maps to NM_000093.3 A1675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr9:137655543 C>T maps to NM_000093.3 D665D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:189950499 T>C did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:189916168 C>A maps to NM_000393.3 G936G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:189927593 C>A maps to NM_000393.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:10084443 G>A maps to NM_015719.3 A1200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr21:47422158 G>C maps to NM_001848.2 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:47546005 C>T maps to NM_001849.3 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:238277715 G>A maps to NM_004369.3 R1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:238285987 C>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr2:238263550 G>A maps to NM_004369.3 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:238283094 C>G maps to NM_004369.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:238289579 C>T maps to NM_004369.3 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:238289867 T>C maps to NM_004369.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:130159394 A>C maps to ENST00000312481 P2071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:130188023 G>A maps to ENST00000312481 W2392*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-56-6546-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:130174343 C>T maps to ENST00000312481 F2208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:130174502 C>A maps to ENST00000312481 L2261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:130380523 C>T maps to NM_001102608.1 P1958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr3:130282212 C>A maps to NM_001102608.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:130318602 C>A maps to NM_001102608.1 G1534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:130293256 C>T maps to NM_001102608.1 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:130340678 C>T maps to NM_001102608.1 P1610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr3:130289870 G>T maps to NM_001102608.1 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:48612108 C>T did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr3:48627134 C>T maps to NM_000094.3 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:48628959 G>A maps to NM_000094.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr3:48612665 C>A maps to NM_000094.3 G2064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:48604104 C>T maps to NM_000094.3 E2764E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:48627115 G>A maps to NM_000094.3 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr3:99514449 G>T maps to ENST00000429802 G570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:99509630 G>A maps to ENST00000429802 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:70935638 G>A maps to NM_001851.4 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr6:70970386 G>T maps to NM_001851.4 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr6:71003995 A>G maps to NM_001851.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr6:70993460 A>G maps to NM_001851.4 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:40775612 G>A maps to NM_001852.3 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:40767499 C>A maps to NM_001852.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:61460129 G>A maps to NM_001853.3 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:120118126 G>A maps to NM_006438.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr8:120118072 C>T maps to NM_006438.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:3691113 A>T maps to ENST00000418971 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:3691563 C>T maps to ENST00000418971 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:346393 A>G maps to NM_130386.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr18:348086 C>G maps to NM_130386.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:334951 C>A maps to NM_130386.2 G536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr18:335078 G>A maps to NM_130386.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr3:15499734 G>A maps to NM_005677.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr2:62227990 G>A maps to NM_152516.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:62228005 C>T maps to NM_152516.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:115628184 G>A maps to NM_016144.2 *203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr20:31291228 C>A maps to NM_053041.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:36296265 C>A maps to NM_014186.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:18895873 G>A maps to NM_000095.2 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:18897347 C>T maps to NM_000095.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:160281808 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:14480173 A>C maps to NM_001144061.1 G902G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr11:14501233 G>A maps to NM_001144061.1 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:14480145 C>A maps to NM_001144061.1 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:128987830 G>T maps to NM_016128.3 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr3:128976392 G>A maps to NM_016128.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:130295840 T>C maps to NM_012133.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr15:49429424 C>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr15:49425957 T>A maps to NM_001143887.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr17:17158244 T>C maps to NM_003653.3 L317L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-22-5485-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr17:17179476 C>T maps to NM_003653.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr8:67971610 C>G maps to NM_006837.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:99688909 C>T maps to NM_006833.4 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:54739299 G>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr12:54741804 C>A maps to NM_016057.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr17:46105864 G>A maps to NM_016429.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:198327403 G>T maps to NM_025147.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr2:198338506 A>G maps to NM_025147.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:131087482 G>A maps to NM_016035.3 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr12:120960137 C>T maps to NM_032314.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:120966932 G>A maps to NM_032314.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:47597739 A>T maps to NM_006587.2 *1043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr4:47655609 G>A maps to NM_006587.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:47765445 C>A maps to NM_006587.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr4:47605630 A>G maps to NM_006587.2 H865H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr4:47602229 C>G did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr4:47667113 G>A maps to NM_006587.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr12:109042779 C>A maps to ENST00000420959 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr17:27944060 C>T maps to ENST00000431377 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:4415024 G>A maps to NM_024535.3 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr16:4415001 A>T did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr16:4407254 G>A maps to NM_024535.3 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr17:13977643 C>T maps to NM_001303.3 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr17:13980209 G>A maps to NM_001303.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr7:1009036 C>A maps to NM_001031617.2 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr20:30231264 G>A maps to NM_032609.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr14:93814405 G>A maps to NM_182971.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr3:148925285 G>A maps to NM_000096.3 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:148895719 G>A maps to NM_000096.3 H975H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:148896346 T>C maps to NM_000096.3 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr3:148917541 G>A maps to NM_000096.3 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:148597672 T>C maps to NM_001870.2 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr3:148596535 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:129939245 T>C did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:68430213 G>T maps to NM_020361.4 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr8:68423883 G>T maps to NM_020361.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr19:17085975 T>C maps to ENST00000443236 Q724Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:148552406 C>G maps to NM_001871.2 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:148552386 A>T maps to NM_001871.2 K84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:148552343 C>T maps to NM_001871.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr15:83224680 G>T maps to ENST00000261723 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:175306945 C>T maps to NM_001008220.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:69265736 C>G did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr12:69250351 T>C maps to NM_001874.4 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:194062501 G>T maps to NM_001080513.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:194062992 G>A maps to NM_001080513.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:194062579 G>A maps to NM_001080513.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:34219077 G>A maps to NM_003915.5 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr16:57151475 G>A maps to NM_152727.5 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:131300446 G>T maps to ENST00000502818 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:36714346 G>A maps to NM_020939.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr16:89650452 C>A maps to NM_014427.4 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:89662917 C>A maps to NM_014427.4 C597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:89655133 C>T maps to NM_014427.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:39124150 G>A maps to NM_153634.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:98304460 C>A maps to NM_000097.5 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:211502424 G>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:211464181 C>G maps to NM_001122633.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:211342490 G>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:211542648 C>T maps to NM_001122633.1 R1487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:145623968 G>A maps to NM_013291.2 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr2:9582062 T>C maps to NM_016207.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:9607845 G>A maps to NM_016207.2 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:68571485 G>C maps to NM_001876.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr11:68549255 G>A maps to NM_001876.3 H445H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:68552316 C>A maps to NM_001876.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr19:50213725 A>G maps to NM_152359.2 Q572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr23:88008874 C>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:88008728 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:88009208 T>C did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:88008901 C>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:88009118 C>A did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:88009034 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:2775966 C>A maps to NM_019609.4 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr20:2778859 C>A maps to NM_019609.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr20:2779184 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:125516830 G>A maps to NM_198148.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr4:8613818 T>C maps to NM_001014447.2 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:8609034 C>A maps to NM_001014447.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:207696962 T>C maps to NM_000651.4 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:207680059 T>C maps to NM_000651.4 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:207700113 A>G maps to NM_000651.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:207741316 C>G maps to NM_000651.4 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:207646141 T>A maps to NM_001006658.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:207647144 G>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:207648283 C>T maps to NM_001006658.2 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:207639949 G>A maps to NM_001006658.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:207641890 A>T maps to NM_001006658.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:78635881 G>T maps to NM_004378.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr1:156670389 C>A maps to NM_001878.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr9:131859549 G>A maps to NM_000755.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:131860613 G>A maps to NM_000755.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:197390730 C>A maps to NM_201253.2 C591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:197398731 C>T maps to NM_201253.2 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:197390691 G>T maps to NM_201253.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:197390148 C>T maps to NM_201253.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr9:126133397 C>A maps to NM_173689.5 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr7:65617209 G>T maps to ENST00000450043 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:65617274 A>G maps to NM_014478.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:35736298 G>T maps to NM_006368.4 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr7:28857734 G>A maps to NM_182898.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:28844105 A>T maps to NM_182898.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr16:3820623 G>A maps to NM_004380.2 Q943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr16:3830745 G>A maps to NM_004380.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr16:3832750 G>A maps to NM_004380.2 Q503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr16:3832793 G>T maps to NM_004380.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr16:3828021 C>T maps to NM_004380.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr16:3823883 A>G maps to NM_004380.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:9986196 C>T maps to NM_001077415.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr22:50318060 G>T maps to NM_001135101.1 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr10:35500641 C>T maps to ENST00000429130 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr10:35500643 A>C maps to ENST00000429130 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:35467821 A>T maps to ENST00000429130 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:76249896 C>T maps to NM_001882.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr17:43893943 C>T maps to NM_001145146.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:43912063 C>T maps to NM_001145146.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:30706894 C>G maps to ENST00000348438 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr14:105945786 C>G maps to ENST00000483017 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr6:43275416 G>A maps to ENST00000449267 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:49814307 G>C maps to NM_001131.2 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:49806192 G>A maps to NM_001131.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:49803028 C>A maps to NM_001131.2 *250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:49676879 A>T maps to ENST00000211238 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr6:49704214 G>T maps to NM_001190986.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr6:49696508 G>A maps to NM_001190986.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:84906689 C>T maps to NM_031476.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr22:21288525 A>C maps to NM_005207.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr22:21288202 C>T maps to NM_005207.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:1321371 G>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:1325353 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:1314964 A>T did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:1325341 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:29131048 G>C maps to NM_015986.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr4:5868447 G>T maps to NM_001014809.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:5837708 G>T maps to NM_001014809.1 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr20:20033045 G>A maps to NM_016652.4 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:152382342 C>T maps to NM_016190.2 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:152382452 C>A maps to NM_016190.2 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:152383037 G>A maps to NM_016190.2 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:17281809 G>T maps to NM_014675.3 E1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:17250857 C>T maps to NM_014675.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:87027959 G>C maps to NM_001143935.1 *641Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:87005146 C>T maps to NM_001143935.1 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr10:99683112 G>T maps to NM_018058.4 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr10:99677371 G>C maps to NM_018058.4 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr11:122720809 C>A maps to NM_019604.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr19:18876307 C>G maps to NM_001098482.1 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:18864379 A>G maps to NM_001098482.1 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:91185215 G>A maps to NM_022769.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr15:91157682 A>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:91162996 C>A maps to NM_022769.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr19:48342761 G>A maps to NM_000554.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:48343179 C>T maps to NM_000554.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:45889224 A>T maps to NM_021117.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:219857817 A>G maps to NM_057094.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr22:25601323 C>T maps to NM_004076.3 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:186256663 C>A maps to NM_017541.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr13:20978772 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:21278977 C>T maps to NM_001888.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:75175780 C>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:56667526 G>T maps to NM_004077.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr12:53565180 G>A maps to NM_015989.4 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:53553950 G>A maps to NM_015989.4 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:10853927 C>A maps to NM_003651.4 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr20:47711382 C>T maps to NM_001316.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:110460060 C>A maps to NM_000757.4 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:149449568 G>A maps to NM_005211.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:1424404 T>A did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:1428350 G>C did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:1401639 A>C did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:1424411 G>C did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:1407770 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:1404668 A>T did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:1409283 G>A did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:1409237 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:37322028 G>A maps to ENST00000262825 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:37328924 G>A maps to ENST00000262825 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr22:37333899 G>T maps to ENST00000262825 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr22:37333577 C>T maps to ENST00000262825 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr22:37333985 C>A maps to ENST00000262825 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr8:19315989 G>A maps to NM_018371.4 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr8:19362937 G>C maps to NM_018371.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:61950642 C>A maps to NM_020991.3 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:75094050 C>T maps to NM_004383.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr15:75091699 C>T maps to NM_004383.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:2808738 C>T maps to NM_033225.5 G3366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:3047578 C>T maps to NM_033225.5 R1751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr8:2813174 C>G maps to NM_033225.5 G3310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:2815330 T>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr8:3216710 G>T maps to NM_033225.5 G1089G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr8:4494991 G>A maps to NM_033225.5 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:3087749 G>C maps to NM_033225.5 S1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:2964164 T>C did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr8:3245034 G>A maps to NM_033225.5 H921H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:4495077 G>A maps to NM_033225.5 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:3008985 G>T maps to NM_033225.5 P1988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr8:3008928 G>T maps to NM_033225.5 P2007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:3256998 T>C maps to NM_033225.5 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr8:2796130 C>T maps to NM_033225.5 L3557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr8:2830789 C>G maps to NM_033225.5 G2924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr8:3224704 C>T maps to NM_033225.5 E988E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:3165275 C>A maps to NM_033225.5 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr1:34049274 C>A maps to ENST00000373381 E2363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:34038219 T>A maps to ENST00000373381 K2510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:34190228 G>C maps to ENST00000373381 Y884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:34003177 G>T maps to ENST00000373381 S3181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr1:34190219 C>T maps to ENST00000373381 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr1:34066582 C>T maps to ENST00000373381 R2206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:34174706 G>A maps to ENST00000373381 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:34006907 G>T maps to ENST00000373381 V3053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:34401427 G>A maps to ENST00000373381 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:34209096 C>A maps to ENST00000373381 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:34052158 C>G maps to ENST00000373381 L2292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:34071502 G>T maps to NM_052896.3 V2103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:113299318 C>T maps to NM_198123.1 W3102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:113564925 C>A maps to NM_198123.1 G1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:114290920 G>A maps to NM_198123.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr8:113484892 T>G maps to NM_198123.1 L1774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr8:113304883 C>A maps to NM_198123.1 G2890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr8:113418956 C>A did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr8:113649187 A>G maps to NM_198123.1 G1191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr8:113301659 A>G maps to NM_198123.1 L3028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr8:113299461 C>A maps to NM_198123.1 G3054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr8:113275907 T>C maps to NM_198123.1 V3274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr8:113988089 C>A maps to NM_198123.1 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:113363402 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:113871397 G>A maps to NM_198123.1 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr8:113694722 A>T maps to NM_198123.1 C875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr8:113314134 G>T maps to NM_198123.1 S2776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:114448936 G>C maps to NM_198123.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:113353709 G>C maps to NM_198123.1 Y2216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr8:114326922 C>T maps to NM_198123.1 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:113301646 G>C maps to NM_198123.1 S3032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:114031359 C>T maps to NM_198123.1 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr8:113563038 T>A maps to NM_198123.1 P1475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:113651003 G>T maps to NM_198123.1 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:113256632 G>T maps to NM_198123.1 P3464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:113569046 G>A maps to NM_198123.1 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr8:113266517 A>T maps to NM_198123.1 P3358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:113317124 G>A maps to NM_198123.1 I2697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:113649183 G>T maps to NM_198123.1 R1193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:113569138 C>A maps to NM_198123.1 G1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr8:113303771 C>A maps to NM_198123.1 G2981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr8:113564903 A>T maps to NM_198123.1 L1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr8:113657356 A>T maps to NM_198123.1 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr8:113668570 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr8:113318349 G>T maps to NM_198123.1 R2653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:113304919 A>T maps to NM_198123.1 P2878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr8:113301693 A>C maps to NM_198123.1 T3016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr8:113243772 C>A did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr8:113347703 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr8:113529361 G>A maps to NM_198123.1 Q1553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr8:114290851 A>G maps to NM_198123.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr8:113484876 T>A maps to NM_198123.1 K1780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr4:71115031 T>C maps to NM_005212.2 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr5:148930406 C>A maps to NM_001025105.1 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:37679191 G>A maps to NM_145203.5 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr17:80211075 C>A maps to NM_001893.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr15:64551399 C>A maps to NM_022048.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr19:1978855 A>T did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:75982088 C>A maps to NM_001897.4 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:75968835 G>T maps to NM_001897.4 G2008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:75979664 G>T maps to NM_001897.4 I1247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:75982631 G>T maps to NM_001897.4 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr3:47618714 G>T maps to ENST00000383738 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr3:47614276 G>T maps to ENST00000383738 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr3:39185791 G>A maps to NM_033027.3 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr12:51470287 G>A maps to NM_030809.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:166535935 C>T maps to ENST00000409420 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr20:23731347 G>T maps to NM_001898.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr20:23731326 G>T maps to NM_001898.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr20:23433295 G>T maps to NM_130794.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr20:23433376 G>T maps to NM_130794.1 Y24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:23666596 G>A maps to NM_001899.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr20:23669510 A>T maps to NM_001899.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr20:23667744 C>A maps to NM_001899.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr20:23666548 G>C maps to NM_001899.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:23472423 C>T maps to NM_005492.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:23472432 C>T maps to NM_005492.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:100077294 C>G did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:100077359 A>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:100087735 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:23424650 C>A maps to NM_138283.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:153880865 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:153880850 G>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:153880851 A>C did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:153880860 A>G did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:153880868 C>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr18:19997753 A>C maps to NM_172241.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr18:19995851 A>G maps to NM_172241.2 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr14:39772704 A>T maps to ENST00000396158 K319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:67671756 C>G maps to NM_006565.3 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr16:67662442 A>G maps to NM_006565.3 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr20:56098951 G>A maps to ENST00000423479 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr18:77470344 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr18:77477824 G>A maps to NM_004715.3 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr18:77475421 G>C maps to NM_004715.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:219267952 A>T did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:204732709 G>T maps to NM_005214.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:204737533 G>T maps to NM_005214.3 *224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:138268335 C>T maps to ENST00000355078 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr5:138260945 C>T maps to ENST00000355078 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:79971514 G>A maps to ENST00000402739 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:79971646 T>A maps to ENST00000402739 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:79878771 A>T maps to ENST00000402739 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr2:79878771 A>C maps to ENST00000402739 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:79971589 A>G maps to ENST00000402739 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:80620417 T>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:80801372 C>T maps to ENST00000402739 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:79971592 T>G maps to ENST00000402739 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:80782968 G>A maps to ENST00000402739 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:80782830 G>A maps to ENST00000402739 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:80085137 G>T did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr10:68979520 A>G maps to NM_013266.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:68040263 T>C maps to NM_013266.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr10:68040353 C>A maps to NM_013266.2 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr10:68979439 T>G maps to NM_013266.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr10:67680255 C>A maps to NM_013266.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr10:67863008 T>G did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr9:111734972 C>T maps to NM_003798.2 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr9:111732693 C>A maps to NM_003798.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr3:41278136 G>A maps to NM_001904.3 K671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:57571192 T>G maps to NM_001085458.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr11:57575872 C>T maps to NM_001085458.1 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:11082930 G>A maps to NM_001332.2 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:11411723 G>T maps to NM_001332.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:11082904 G>T maps to NM_001332.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:11384825 C>A maps to NM_001332.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr5:11732317 A>T maps to NM_001332.2 L35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr5:11346611 C>A maps to NM_001332.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:11199611 C>G maps to NM_001332.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:11384927 G>A maps to NM_001332.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:11117663 G>A maps to NM_001332.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:11159740 C>T maps to NM_001332.2 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr17:3563243 G>A maps to NM_001031681.2 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:16685638 G>C did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr1:15769955 G>C maps to NM_007272.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr20:44526354 G>C did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr11:88029409 T>G maps to NM_001814.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:1775092 C>A maps to NM_001909.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:206331025 C>T maps to ENST00000361052 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:66333158 G>T maps to NM_003793.3 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:25043645 C>T maps to NM_001911.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:150772181 C>A maps to NM_000396.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:150779233 C>A maps to NM_000396.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr9:90345350 G>T maps to NM_145918.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:99797039 C>T maps to NM_001333.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr4:156863507 C>T maps to NM_001334.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:150724427 C>T maps to NM_004079.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr11:65648992 T>G did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr20:57581518 C>T maps to NM_001336.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr20:57576577 G>T maps to NM_001336.3 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:70277369 C>A maps to NM_001184740.1 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr7:117431825 G>T maps to NM_033427.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr7:117450848 C>T maps to NM_033427.2 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:117432358 T>G maps to NM_033427.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr7:117431716 T>C maps to NM_033427.2 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:112999475 G>A maps to NM_018704.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr16:88781040 G>A maps to ENST00000378384 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr16:88779196 G>T maps to ENST00000378384 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:16867060 G>A maps to NM_001081.3 F3595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:17032458 G>A maps to NM_001081.3 P1408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:17087149 G>A maps to NM_001081.3 F1176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr10:16990573 A>T maps to NM_001081.3 P1704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr10:17157564 G>A maps to NM_001081.3 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr10:17156038 C>A maps to NM_001081.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:17026275 G>A maps to NM_001081.3 I1451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:17087131 C>G maps to NM_001081.3 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr10:17024566 A>C maps to NM_001081.3 S1537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr10:16882992 G>C maps to NM_001081.3 S3239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:16911749 G>A maps to NM_001081.3 C3113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr17:55948727 G>T maps to NM_017949.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr7:148485761 A>G maps to NM_003592.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr10:35333789 A>C maps to NM_001198778.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr10:35324156 C>T maps to NM_001198778.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr2:225376241 C>A maps to NM_003590.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:225367789 C>T did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr2:225376189 G>C maps to NM_003590.3 S255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:225449699 G>A maps to NM_003590.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr2:225346607 C>T did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr2:225378356 T>C did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:119693973 C>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:119694096 T>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:119680456 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:119660630 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:119664004 G>T did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:107920720 A>G maps to NM_003478.3 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:43008366 C>A maps to NM_001168370.1 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:43172101 G>T maps to ENST00000354495 A1388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr6:43189038 G>A maps to ENST00000354495 E2244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr6:43189467 C>G maps to ENST00000354495 L2266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr6:43181258 G>T maps to ENST00000354495 G1814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:43155791 G>T maps to ENST00000354495 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:43163985 G>A maps to ENST00000354495 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:43155590 G>A maps to ENST00000354495 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:101801837 A>G did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr7:101747622 G>C maps to ENST00000360264 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr7:101870949 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:101840335 G>T maps to ENST00000360264 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:111744783 G>A maps to NM_015267.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:111779755 C>T maps to NM_015267.3 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:111785936 C>T maps to NM_015267.3 S1423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr12:111758476 C>T maps to NM_015267.3 Y888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr12:111729336 C>T maps to NM_015267.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:111748469 C>T maps to NM_015267.3 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr10:124596491 C>T maps to NM_022034.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:124594349 C>T maps to NM_022034.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:180815460 T>C did not map to a codon.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:36958421 C>A maps to NM_017748.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:36958999 C>A maps to NM_017748.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr11:107288982 C>A maps to NM_152434.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr11:107300079 G>C maps to NM_152434.2 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:107288943 G>A maps to NM_152434.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:49052863 C>T maps to NM_025087.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr4:49052818 G>C maps to NM_025087.2 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr4:49009278 G>A maps to NM_025087.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr4:49005875 G>A maps to NM_025087.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr4:49005779 C>A maps to NM_025087.2 Y277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:57416880 G>C maps to NM_002996.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:76943559 C>T maps to NM_001565.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr10:44880405 G>C maps to NM_001178134.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr5:134914176 C>G maps to NM_004887.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:74964370 A>G maps to NM_002089.3 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr4:74702937 G>A maps to NM_002993.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:219029166 C>A maps to NM_000634.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:219000267 G>A maps to NM_001168298.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:219000498 C>T maps to NM_001168298.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:70836892 G>C did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:70836521 C>A did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:136873259 G>A maps to NM_001008540.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:136873422 C>T maps to NM_001008540.1 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr4:105412320 G>A maps to NM_025212.1 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:139060755 C>T maps to NM_016463.7 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:30578031 C>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:30578233 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:30577645 A>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:30577740 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:30577969 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:30578450 T>C did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:35969925 G>C did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:35985768 A>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:35993796 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:35974214 A>C did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr23:35974178 A>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:19983479 T>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:19947937 G>C did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:19968910 C>T did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:75397616 G>C did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:75394774 C>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:45060019 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:45013206 C>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:106462112 G>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:106466059 A>G did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr23:134303629 G>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:118699257 C>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:105855547 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:105865894 T>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:105868449 G>T did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:105855369 G>T did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:36156568 C>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:36083859 G>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:36103514 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:36117964 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:36117868 C>G did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:36116910 G>T did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:115593068 C>A did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:115593950 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:70323873 C>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:70323956 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:139038192 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:139038631 G>C did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:139038431 C>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:139038092 A>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:139047575 G>C did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:139038228 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:139038711 T>C did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:139038260 T>A did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr17:61513430 G>A maps to NM_001915.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:202936318 C>T maps to NM_016243.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:43024194 G>A maps to NM_001171660.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr22:43023324 C>A maps to NM_001171660.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:37658244 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:37670074 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:37663198 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:37670106 C>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:37642780 G>C did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:37663353 G>T did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:37663380 T>G did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:172398275 G>C maps to NM_024843.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr8:145152202 G>A maps to NM_001916.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr8:145150844 C>A maps to NM_001916.3 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr15:22940826 G>C maps to NM_014608.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr5:156819908 G>A maps to ENST00000442283 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr5:156766091 C>A maps to ENST00000442283 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr5:156757806 G>A maps to ENST00000442283 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:156787315 G>T maps to ENST00000442283 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr17:74527628 C>A maps to NM_134268.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:83128725 C>G did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:83128573 G>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:83128310 G>C did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:83128461 T>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:83128682 A>G did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:83128918 G>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:83128431 C>G did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:83128188 C>A did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:83129186 G>C did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:83129611 A>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr9:105765445 A>G maps to NM_001340.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:105767116 G>T maps to NM_001340.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:105767645 G>T maps to NM_001340.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr16:50826617 T>A did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr16:50825601 G>T did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr8:143996632 A>G maps to NM_000498.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr10:104594715 G>A maps to NM_000102.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:75014672 C>A maps to NM_000499.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr15:75047332 G>A maps to NM_000761.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr2:72360205 C>A maps to NM_019885.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr10:94824181 C>T maps to NM_183374.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:219679731 G>A maps to NM_000784.3 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:41597755 G>T maps to NM_000766.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:41594546 C>A maps to NM_000766.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:41594859 C>T maps to NM_000766.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:41594426 G>A maps to NM_000766.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr19:41594402 G>A maps to NM_000766.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr10:96493184 T>A maps to NM_000772.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr10:96447969 C>T maps to NM_000772.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:96522509 C>T maps to NM_000769.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr10:96522557 C>A maps to NM_000769.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:96798717 A>G maps to NM_000770.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr10:96745812 G>C maps to NM_000771.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr22:42523976 C>T maps to NM_000106.4 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr22:42522958 C>T maps to NM_000106.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr10:135342028 G>T maps to NM_000773.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr10:135345140 G>T maps to NM_000773.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:41627462 G>T maps to NM_000774.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr19:41627405 C>A maps to NM_000774.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr19:41630711 G>C maps to NM_000774.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:41703717 G>A maps to ENST00000301173 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr7:1026300 G>A maps to NM_017781.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr7:99367428 C>T maps to NM_017460.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:99441865 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:99250243 C>T maps to NM_000777.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:99313519 C>T maps to ENST00000292414 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:100157447 G>A maps to NM_006668.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:100188384 C>T maps to NM_006668.1 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:100173915 G>A maps to NM_006668.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr14:100166357 C>T maps to NM_006668.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr14:100173936 G>T maps to NM_006668.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:47607783 C>G maps to NM_001010969.2 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr1:47614360 C>T maps to NM_001010969.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr19:16024571 C>A maps to NM_021187.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr19:16035632 G>A maps to NM_021187.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:16032945 C>T maps to NM_021187.3 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:16008361 C>A maps to NM_001082.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:15997052 C>T maps to NM_001082.3 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr19:15989679 G>A maps to NM_001082.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:15989694 C>T maps to NM_001082.3 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:16000382 G>A maps to NM_001082.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:15769355 G>A maps to NM_000896.2 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:15770158 G>A maps to NM_000896.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:15760020 G>T maps to NM_000896.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr19:15760758 C>A maps to NM_000896.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:15739590 C>T maps to NM_007253.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:91755661 G>C maps to NM_000786.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr8:59404138 T>A maps to NM_000780.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr8:59409686 A>T maps to NM_000780.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:59410831 T>A maps to NM_000780.3 K93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr8:65517286 G>T maps to NM_004820.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr8:65527679 G>A maps to NM_004820.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:77528614 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:77528441 C>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:77528292 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:49281180 C>T maps to NM_020377.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr13:49281472 C>T maps to NM_020377.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr13:49281312 C>G maps to NM_020377.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr13:49281660 G>T maps to NM_020377.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:76694408 C>A maps to NM_004762.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr22:37707537 G>A maps to NM_013385.3 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:37692054 G>A maps to NM_013385.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:37693654 C>T maps to NM_013385.3 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:24718053 C>G maps to NM_015330.2 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr21:27852618 A>T maps to ENST00000435845 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:242674878 G>A maps to NM_152783.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:4419020 C>A maps to NM_001040101.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr6:39846264 G>C maps to ENST00000398904 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:57602254 G>A maps to ENST00000371231 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:57476448 C>T maps to ENST00000371231 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr5:39383249 G>A maps to NM_001343.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:72053448 C>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr13:72014821 C>A maps to ENST00000359684 G750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:86068159 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:85906065 C>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:86068251 A>C did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:85994852 C>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:86067938 G>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:85906110 A>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:86067948 G>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:85631864 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:85906091 A>G did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:86069819 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:59112967 G>T maps to NM_016651.5 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:59113531 G>T maps to NM_016651.5 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr14:59113809 C>G maps to NM_016651.5 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:61511222 C>T maps to NM_006133.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:61490430 C>G maps to NM_006133.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:6464442 C>A maps to NM_139179.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr3:49053092 A>G maps to NM_001009996.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:109292473 G>T maps to NM_001917.4 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr13:106142325 A>T maps to NM_172370.3 K120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:155701181 G>A maps to NM_004632.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:155701790 G>A maps to NM_004632.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr9:90321439 C>T maps to NM_004938.2 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr9:90313661 G>A maps to NM_004938.2 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:90312078 C>G maps to NM_004938.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:3959563 C>T maps to NM_001348.1 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:3959146 G>A maps to NM_001348.1 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr4:100784937 A>G maps to NM_014395.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr4:100774444 G>C maps to NM_014395.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:136701010 C>A maps to NM_001349.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:173826782 G>C maps to NM_018122.4 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr1:173802511 A>G did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:173806113 G>T maps to NM_018122.4 G234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:173800687 G>T maps to NM_018122.4 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:16636038 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:16636045 T>A maps to NM_001190811.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr9:122075417 G>T maps to NM_014618.2 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr9:122004336 A>T maps to NM_014618.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr9:121971118 G>T maps to NM_014618.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr9:122075432 G>T maps to NM_014618.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr17:42809610 A>G maps to NM_145663.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr20:44037163 G>A maps to NM_001048225.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:44099660 T>C maps to NM_001122956.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:137893469 G>A maps to NM_016216.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:137892434 G>A maps to NM_016216.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:100681746 C>T maps to NM_001918.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr11:20181579 A>C maps to ENST00000227256 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:20177906 G>A maps to ENST00000227256 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:45429898 T>G did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:45410158 T>A maps to NM_001004329.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr9:37861492 G>A maps to NM_024345.3 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:125685297 A>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:125685489 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:125685717 C>A did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr23:125685916 G>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:125685378 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:125686049 G>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:125685529 C>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:125686326 C>A did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr23:125686547 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:125685516 A>G did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:125686401 C>A did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:125686111 G>A did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr23:125686397 G>A did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr23:125685454 G>C did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:125298855 G>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:125299534 C>G did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:125299304 G>C did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:125298565 C>G did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr23:125299016 C>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:125299527 G>A did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:104427349 G>C maps to NM_015420.6 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:104427541 A>T maps to NM_015420.6 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:14065388 C>G maps to NM_138353.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr14:73425437 G>T maps to NM_015604.3 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:73412708 G>T maps to NM_015604.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr4:41984870 C>A maps to NM_001029955.3 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:88885347 G>A maps to NM_152418.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr8:88885770 C>A maps to NM_152418.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr8:88885962 C>A maps to NM_152418.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:88885554 C>G maps to NM_152418.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr8:88885461 C>A maps to NM_152418.3 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr8:88885714 G>T maps to NM_152418.3 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr14:69521475 G>A maps to NM_003861.2 Q643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:69585938 C>A maps to NM_003861.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:168012379 T>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:160209782 C>A maps to NM_015726.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:27998520 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:27998446 G>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:27998848 G>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:27997795 C>A did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:27998326 T>A did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:27998339 T>C did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:27998585 G>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:27999273 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:27997797 C>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:27999093 A>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:117858345 A>T did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr6:117862183 C>T maps to ENST00000338728 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:50432549 C>T maps to NM_005215.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr18:50705329 A>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr18:50683759 C>A maps to NM_005215.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr18:50278667 G>A maps to NM_005215.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr18:50731682 A>T maps to NM_005215.3 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr18:50977005 C>A maps to NM_005215.3 T1122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr18:50592438 T>A maps to NM_005215.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:50961578 G>T maps to NM_005215.3 E1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr12:55042030 G>A maps to NM_053283.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:31327850 C>A maps to NM_181807.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:24278331 C>T maps to NM_016356.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr6:24205304 T>A maps to NM_016356.3 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:24178826 C>A maps to NM_016356.3 G353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:32678368 C>A maps to NM_001099434.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:6649924 G>A maps to NM_003737.2 P1766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:6651035 G>A maps to NM_003737.2 V1634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr11:6653339 C>A maps to NM_003737.2 G1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr11:6661830 C>A maps to NM_003737.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:6661602 T>A maps to NM_003737.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:6651097 C>A maps to NM_003737.2 E1614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:6651119 C>A maps to NM_003737.2 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:6661841 G>T maps to NM_003737.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:6650039 G>T maps to NM_003737.2 S1728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:155278420 C>T maps to NM_017639.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr4:155156161 C>T maps to NM_017639.3 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:155219785 C>A maps to NM_017639.3 E1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr4:155156791 C>A maps to NM_017639.3 V2549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr4:155237113 C>T maps to NM_017639.3 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:155156646 G>A maps to NM_017639.3 Q2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:155254548 G>T maps to NM_017639.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:155253954 G>A maps to NM_017639.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:155249255 G>C maps to NM_017639.3 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:151153968 G>T maps to NM_001040261.4 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:36759618 G>A maps to NM_033403.1 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:36756940 G>A maps to NM_033403.1 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:91552163 G>A maps to NM_133503.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr12:91550873 G>T maps to NM_133503.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:155019727 C>T maps to NM_152494.3 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr1:155007171 A>G maps to NM_152494.3 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:155006050 G>A maps to NM_144622.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr13:95131311 G>A maps to NM_001129889.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr13:95095743 C>A maps to NM_001129889.1 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:74598705 G>C maps to NM_004082.4 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr2:74605228 G>A maps to NM_004082.4 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr8:30040644 C>T maps to NM_006571.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr3:182681667 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:182679085 C>A maps to NM_020640.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:182679094 C>A maps to NM_020640.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr13:114112391 T>C maps to NM_001014283.1 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:20873629 C>T maps to NM_173475.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:110574146 C>T did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:110653547 G>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:110644423 T>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:110653370 C>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:110644548 T>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:110644365 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:79994268 C>G maps to NM_016286.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:17426740 A>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:31695070 C>T maps to NM_013974.1 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:31695430 C>G maps to NM_013974.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:31696794 C>A maps to NM_013974.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:61071504 C>T maps to NM_001923.3 V888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:61081071 G>T maps to NM_001923.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:61070588 C>A maps to NM_001923.3 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:61070620 G>T maps to NM_001923.3 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr11:47259386 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:50530991 C>A maps to NM_000790.3 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:50566926 G>A maps to NM_000790.3 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr14:53619564 G>A maps to NM_001160148.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr11:103908026 G>A maps to NM_001001711.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr11:103907804 A>G maps to NM_001001711.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:57910714 C>T maps to NM_001195056.1 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:74034807 C>G maps to NM_019058.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:101109181 G>A maps to NM_145244.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr12:49391374 C>T maps to NM_015086.1 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:162745570 C>T maps to NM_006182.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:162724626 G>T maps to NM_006182.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:15770897 A>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:15770166 G>T maps to NM_004939.1 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:15770901 G>T maps to NM_004939.1 G699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr2:15767205 A>T maps to NM_004939.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:108547816 G>T maps to NM_004398.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:31241997 A>G maps to NM_030653.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr12:31249832 G>A maps to NM_030653.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr22:38894558 C>T maps to NM_001098504.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:70400754 C>T maps to NM_018332.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:70719869 G>A maps to NM_004728.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:49230474 C>G maps to NM_004818.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr14:94545632 T>A maps to NM_020414.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:134681115 T>C did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr20:47835939 C>T maps to NM_017895.7 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr20:47835946 C>T maps to NM_017895.7 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr20:47849861 G>T maps to NM_017895.7 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr9:135470305 T>A maps to NM_022779.7 R835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr9:135538024 G>T maps to NM_022779.7 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr23:41204466 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:41201856 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:41204662 G>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr24:15023842 G>C did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:176939831 C>A maps to NM_016222.2 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:176943820 C>A maps to NM_016222.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:74104639 C>T maps to NM_018665.2 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr5:134143583 G>T maps to ENST00000452510 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr5:134153323 G>T maps to ENST00000452510 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:35993347 G>A maps to NM_007010.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:23019970 A>T did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr23:23019067 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:23018667 A>G did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:23019931 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:23018430 A>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:23018537 G>C did not map to a codon.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr23:23019366 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:23018386 A>G did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:113612733 C>A maps to NM_001111322.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:113601993 G>A maps to NM_001111322.1 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr12:113603448 C>A maps to NM_001111322.1 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr12:113612522 C>A maps to NM_001111322.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:44613193 G>A maps to NM_019082.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:44608557 G>T maps to NM_019082.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:200635424 G>A maps to NM_001031725.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr4:169195105 G>A maps to NM_017631.5 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:169173722 T>C maps to NM_017631.5 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr4:169157420 G>A maps to NM_017631.5 F1505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:169158918 G>A maps to NM_017631.5 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr4:169204617 C>G maps to NM_017631.5 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:169197294 C>T maps to NM_017631.5 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr4:169300556 G>A maps to NM_001012967.1 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr4:169305852 C>G maps to NM_001012967.1 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:90020689 C>T maps to NM_207514.1 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr16:90015914 G>A maps to NM_207514.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:6914137 C>A maps to NM_021010.1 E28*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-34-2600-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:49986760 G>A maps to NM_001037497.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:50011471 G>C maps to NM_001037498.1 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr20:29847260 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:29891154 G>A maps to NM_001037731.1 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr20:29956506 C>T maps to NM_054112.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:29965060 T>A maps to NM_153289.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr20:77048 T>A maps to NM_153325.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr20:139601 G>T maps to NM_139074.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:168637 T>C maps to NM_001037732.1 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr8:11832057 A>G maps to NM_001033018.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:7752263 C>T maps to NM_004942.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:40981203 C>T maps to NM_022774.1 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:40980594 G>T maps to NM_022774.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:126144460 G>A maps to NM_020946.1 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:126414401 T>A maps to NM_020946.1 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr9:126144595 T>G maps to NM_020946.1 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr9:126392754 G>A maps to NM_020946.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:197522229 G>A maps to NM_001195215.1 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:197576298 C>A maps to NM_001195215.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:140301336 G>T maps to NM_015689.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:115137114 G>A maps to ENST00000393274 Q804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:142161911 C>A maps to NM_014957.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr15:65964147 G>A maps to ENST00000443035 F1482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:19316472 C>T maps to NM_017925.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr9:19341086 A>T maps to NM_017925.4 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:9167306 G>A maps to NM_015213.2 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:9167294 T>C maps to NM_015213.2 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:68949738 A>G maps to NM_001114120.1 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:68947131 C>A maps to NM_001114120.1 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:59893657 T>C maps to NM_018369.2 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr22:32234676 C>T maps to NM_001136029.1 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr22:32293622 C>T maps to NM_001136029.1 S1444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr22:32302362 G>T maps to NM_001136029.1 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr22:32297746 C>G maps to NM_001136029.1 Y1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr22:32215143 C>T maps to NM_001136029.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr8:120940801 G>C maps to NM_022783.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr11:33053044 C>T maps to NM_001077242.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:124054245 G>A maps to NM_024295.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr2:220290421 C>G maps to NM_001927.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:220285263 G>A maps to NM_001927.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:220285299 C>A maps to NM_001927.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr15:89074850 G>C maps to NM_017996.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr16:11035741 G>A maps to NM_014015.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:3800106 G>T maps to ENST00000430539 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:3800176 G>T maps to ENST00000430539 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:24749939 C>A maps to NM_001127453.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr9:117186784 C>G maps to NM_015404.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr2:179325084 C>T maps to NM_001042702.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:179325138 G>C maps to NM_001042702.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:179319252 C>T maps to NM_001042702.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:69420306 T>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:69424173 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:56346687 C>T maps to NM_201554.1 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:14217687 C>A maps to NM_004080.2 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:14758224 C>T maps to NM_004080.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:14724924 G>A maps to NM_004080.2 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr2:234347022 C>A maps to NM_152879.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:234365571 T>A maps to NM_152879.2 Y801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:234371380 G>C maps to NM_152879.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:234356820 C>A maps to NM_152879.2 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:234372820 G>C maps to NM_152879.2 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:54912187 C>A maps to NM_003647.2 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:185906144 C>A maps to NM_001346.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:137531209 G>T maps to NM_004717.2 Y133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:137080430 T>G maps to NM_004717.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:137082133 T>A maps to NM_004717.2 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:50121134 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:50130569 T>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:50165517 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:50129356 T>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:50213032 C>T did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:50165474 C>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:50119072 C>G did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:50127722 C>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:50167244 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:50114794 G>T did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:50136226 G>T did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:74154147 G>T maps to NM_080916.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:71146794 G>T maps to NM_001360.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:71155062 G>C maps to NM_001360.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:49442785 G>T maps to NM_014475.3 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:99361611 A>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:49488130 C>A maps to NM_021044.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:12790660 C>A maps to NM_001930.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:24113370 G>T maps to NM_182908.4 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr14:24505723 G>A maps to NM_001082488.1 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr14:24517436 T>A did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr14:24470660 G>C maps to NM_198083.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr17:21075444 C>T maps to NM_015510.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr17:9676194 G>A maps to ENST00000330255 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:2161100 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:2184965 C>A did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:2209582 G>C did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:2184903 A>G did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:2161141 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:12159704 G>T maps to NM_018706.5 G785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:12159704 G>T maps to NM_018706.5 G785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr4:24578073 G>C maps to NM_001358.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr5:54555721 A>G maps to NM_019030.2 D1337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:127555575 G>T maps to NM_018180.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:47883022 G>T maps to NM_014681.5 V921V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:47858495 G>T maps to NM_014681.5 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr20:37620140 G>T maps to NM_021931.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr20:37634943 G>A maps to NM_021931.3 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr12:125473499 G>T maps to NM_032656.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr12:125465137 A>G maps to NM_032656.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:125470743 C>T maps to NM_032656.3 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr12:125435085 G>A maps to NM_032656.3 S998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr16:72141385 G>T maps to NM_014003.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr16:72142151 C>A maps to NM_014003.3 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:39088780 G>A maps to NM_198963.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:39089398 C>A maps to NM_198963.1 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr2:39025485 T>G maps to NM_198963.1 G1372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr17:40260051 C>A maps to NM_024119.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr17:41570100 C>T maps to NM_004941.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr17:41570887 G>C maps to NM_004941.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:182847164 G>A maps to NM_001357.4 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:140958123 G>A maps to ENST00000398557 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:140953217 G>A maps to ENST00000398557 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr5:140953559 A>G maps to ENST00000398557 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:96203954 C>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:96173511 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:95993590 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:96396770 A>G did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:96171547 A>G did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:96684740 C>G did not map to a codon.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr13:60590067 T>C maps to NM_001042517.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr13:60566227 G>A maps to NM_001042517.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:95582906 G>T maps to NM_177438.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr20:61525783 G>A maps to NM_033081.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr20:61528145 C>T maps to NM_033081.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr20:61512600 C>T maps to NM_033081.2 E1569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr20:61512016 G>T maps to NM_033081.2 S1764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr20:61513662 C>T maps to NM_033081.2 R1215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr20:61528076 C>A maps to NM_033081.2 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr5:61690316 T>A maps to NM_014473.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:54371966 G>A maps to NM_000792.5 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:80669492 C>A maps to NM_001007023.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:80669427 G>T maps to NM_001007023.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr21:47971580 G>T maps to ENST00000318711 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr21:47970520 C>T maps to ENST00000318711 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr21:47959841 G>C maps to ENST00000318711 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr21:47918561 C>A maps to ENST00000318711 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:51089047 A>C did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr10:373116 C>A did not map to a codon.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr10:323265 T>A maps to NM_014974.2 *1557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr10:436245 G>A maps to NM_014974.2 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:468775 G>A maps to NM_014974.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:68512320 C>T maps to NM_004675.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:68512773 G>A maps to NM_004675.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:189599467 G>A maps to NM_052952.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr3:122525798 T>C did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:231830301 C>T maps to NM_001164537.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:231885717 C>A maps to NM_001164537.1 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:223178587 C>T maps to NM_032890.2 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:223176709 G>A maps to NM_032890.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:223178401 C>T maps to NM_032890.2 N1221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:40660226 C>A maps to NM_033510.1 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr15:40660490 C>T maps to NM_033510.1 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:111866261 G>T maps to NM_001037954.2 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:111844921 C>T maps to NM_001037954.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr11:111915875 T>A maps to NM_001931.4 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr8:12957577 G>T maps to NM_182643.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr8:12943811 T>G maps to NM_182643.2 R1485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr8:13251103 A>C maps to NM_182643.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr8:12957313 G>A maps to NM_182643.2 H844H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr8:13357322 G>A maps to NM_182643.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:107545939 T>A maps to NM_000108.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr7:107542180 A>G did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr3:38081084 C>T maps to NM_007335.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:38159349 G>A maps to NM_007335.2 E1513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:196792248 C>T maps to NM_004087.2 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:196867070 G>T maps to NM_004087.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:83585512 G>T maps to NM_001142699.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:83673929 G>A maps to NM_001142699.1 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:69712106 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:69665407 G>T did not map to a codon.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:7094077 G>A maps to NM_001365.3 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:7095303 G>A maps to NM_001365.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:7097028 T>A maps to NM_001365.3 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr10:79584219 T>A maps to NM_004747.3 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr18:3534459 G>T maps to NM_004746.2 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr18:3879840 G>T maps to NM_004746.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:1497404 G>A maps to ENST00000357934 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:1616588 C>A maps to ENST00000357934 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:35332750 C>T maps to NM_001080418.1 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:35351751 G>A maps to NM_001080418.1 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr1:35332771 C>T maps to NM_001080418.1 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:35350613 G>A maps to NM_001080418.1 F655F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr1:35351123 C>G maps to NM_001080418.1 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:35060413 C>T maps to ENST00000339266 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr20:35154324 C>T maps to ENST00000339266 I892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr14:55642125 G>A maps to NM_014750.4 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:170592611 C>T maps to NM_005618.3 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:170594016 G>T maps to NM_005618.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr6:170597489 C>T maps to NM_005618.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:75366626 G>A maps to NM_001933.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr2:172951529 T>G maps to NM_178120.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:172967086 G>T maps to NM_004405.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:172965550 G>T maps to NM_004405.3 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr17:48050471 G>T maps to NM_138281.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:96650125 G>T maps to NM_005221.5 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:44685875 C>G maps to NM_019100.4 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr10:124335934 C>T maps to ENST00000368915 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr10:124339202 G>A maps to ENST00000368915 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr10:124353097 G>A maps to ENST00000368915 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr10:124396773 G>C maps to ENST00000368915 T2296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr10:124402787 C>A maps to ENST00000368915 S2501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:31893405 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:32404507 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:32429975 C>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:32583828 C>G did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:31152217 C>A did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:32486703 T>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:32305784 G>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:32429925 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:31525434 T>A did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:31462723 C>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:32383288 T>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:31947804 C>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:32591902 G>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:31196889 G>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:32509415 T>C did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr23:31514964 G>T did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:32328380 C>T did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:32360356 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:31497148 C>A did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:32404523 C>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:31341741 G>A did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:31198491 T>C did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:31893456 T>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:31462721 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:32408278 G>C did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:32360338 C>G did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:32366645 C>T did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:32398797 C>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:32361366 T>G did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:31838128 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:32481677 T>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:31676155 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:31165522 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:31496326 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:32305647 T>C did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:32662321 C>T did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:32662274 C>G did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr19:36002310 A>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr19:36004080 G>T maps to NM_033317.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:1053756 C>T maps to NM_181872.4 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr9:990074 G>C maps to NM_021240.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr9:990422 G>A maps to NM_021240.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr9:22451171 G>T maps to NM_022160.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:53925206 G>A maps to NM_033067.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr19:42353005 G>C maps to ENST00000427618 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr7:86813863 A>G maps to NM_021145.3 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:118485783 C>G maps to NM_005509.4 S1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:118484908 A>G maps to NM_005509.4 K1129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr5:118485539 C>A maps to NM_005509.4 R1340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:51828945 C>A maps to NM_001174116.1 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:70178814 A>G maps to NM_001080449.1 F1067F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr3:52417938 C>A maps to ENST00000273600 T2738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:52360903 G>T maps to ENST00000273600 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:52420189 C>T maps to ENST00000273600 I2880I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr3:52398928 C>T maps to ENST00000273600 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:52361926 G>C maps to ENST00000273600 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr12:124335547 T>A maps to NM_207437.3 P1954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:124311313 C>T maps to NM_207437.3 L1302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:124352551 G>T maps to NM_207437.3 G2351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:124311349 C>T maps to NM_207437.3 G1314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:124297755 C>T maps to NM_207437.3 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:124311322 C>G maps to NM_207437.3 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr12:124257440 G>T maps to NM_207437.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:124272398 C>A maps to NM_207437.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr12:124352115 A>T maps to NM_207437.3 K2306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr7:21721270 G>T maps to NM_003777.3 V1817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr7:21805044 G>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr7:21779281 C>T maps to NM_003777.3 P2642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr7:21584691 T>C maps to NM_003777.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr7:21640752 G>A maps to NM_003777.3 W1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr7:21912963 A>C maps to NM_003777.3 R4021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr7:21584664 G>A maps to NM_003777.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr7:21730457 T>A maps to NM_003777.3 A2007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr7:21778397 C>A maps to NM_003777.3 I2582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:21751445 G>A maps to NM_003777.3 L2324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:21630855 G>T maps to NM_003777.3 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:21757517 C>G maps to NM_003777.3 S2377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr3:57493429 A>C maps to NM_178504.4 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:76455987 C>T maps to ENST00000389840 K3163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:76497288 C>A maps to ENST00000389840 L1806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:76451812 G>C maps to ENST00000389840 A3347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr17:76446778 G>A maps to ENST00000389840 S3614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:7678245 A>C maps to NM_020877.2 P1557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:7705317 C>T maps to NM_020877.2 L2985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:7700549 C>T maps to NM_020877.2 I2640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr17:7667311 C>T maps to NM_020877.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:7643161 G>T maps to NM_020877.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr17:7637983 G>A maps to NM_020877.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:7695335 G>C maps to NM_020877.2 R2334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:21049286 G>A maps to NM_017539.1 I1582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:20976397 G>C maps to NM_017539.1 L2936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr16:21082069 A>G maps to NM_017539.1 C1054C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr16:21065765 C>A maps to NM_017539.1 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr16:21030988 G>T maps to NM_017539.1 P1993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:21093015 G>A maps to NM_017539.1 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr16:20944646 C>T maps to NM_017539.1 L4060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr16:20975047 C>T maps to NM_017539.1 K3386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr16:20994169 G>T maps to NM_017539.1 R2578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr16:20975046 C>A maps to NM_017539.1 E3387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr16:20975911 C>A maps to NM_017539.1 A3098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:13911602 C>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:13885212 G>A maps to NM_001369.2 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr5:13719114 C>T maps to NM_001369.2 A4125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:13770871 C>A maps to NM_001369.2 R3197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr5:13776759 G>C maps to NM_001369.2 S3054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:13770907 A>T maps to NM_001369.2 Y3185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr5:13776796 G>T maps to NM_001369.2 R3042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr5:13845025 G>A maps to NM_001369.2 Q1731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr5:13716739 G>A maps to NM_001369.2 V4255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr5:13867921 G>A maps to NM_001369.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr5:13700923 T>C maps to NM_001369.2 E4516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:13922214 C>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr5:13830717 G>T maps to NM_001369.2 R2017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr5:13919409 G>A maps to NM_001369.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:13735336 G>T maps to NM_001369.2 Y3888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr5:13737391 T>C maps to NM_001369.2 Q3808Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr5:13866337 G>A maps to NM_001369.2 I1369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:84785055 A>T maps to NM_001370.1 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:84784928 C>A maps to NM_001370.1 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:196671472 C>T maps to NM_018897.2 R3389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr2:196756522 T>G maps to NM_018897.2 L1634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr2:196892734 A>G maps to NM_018897.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:196723358 C>A maps to NM_018897.2 E2636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:196689161 T>A maps to NM_018897.2 L3036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:196765212 G>T maps to NM_018897.2 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:196851842 A>G maps to NM_018897.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr2:196688977 C>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:196726626 A>T maps to NM_018897.2 L2517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:196737066 G>T maps to NM_018897.2 L2180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:196636524 G>A maps to NM_018897.2 F3764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:196620854 A>C did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:196619070 A>T maps to NM_018897.2 P3918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:196822071 T>A maps to NM_018897.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:38941581 T>A maps to ENST00000327475 L4212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr6:38879312 T>A maps to ENST00000327475 Y3258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr6:38704870 C>A maps to ENST00000327475 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:38835932 T>A maps to ENST00000327475 I2251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:38835953 T>C maps to ENST00000327475 D2258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr6:38793995 G>C maps to ENST00000327475 L1292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr6:38939382 C>A maps to ENST00000327475 S4144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:38913255 G>A maps to ENST00000327475 L3995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:38819389 T>C maps to ENST00000327475 F1790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:38851096 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:11572549 C>T maps to NM_001372.3 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:11687648 G>T maps to NM_001372.3 P2618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:11666768 C>A maps to NM_001372.3 I2336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr17:11603085 C>G maps to NM_001372.3 A1637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:11726141 A>T maps to NM_001372.3 K3013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:11631151 C>A maps to NM_001372.3 Y1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr17:11837288 C>A maps to NM_001372.3 Y4130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:11532900 G>C maps to NM_001372.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:11835351 C>A maps to NM_001372.3 R4043R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr17:72305466 C>T maps to NM_023036.4 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr17:72285876 T>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr16:46998597 G>A maps to NM_005880.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr16:46991041 G>T maps to NM_005880.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:73670543 A>T maps to NM_153614.2 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:220147634 C>T maps to NM_006736.5 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr2:234652361 G>A maps to NM_001001394.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:234652403 G>A maps to NM_001001394.3 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:22171303 A>G maps to NM_022365.3 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:183608386 G>A maps to NM_018981.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:183595822 C>G maps to NM_018981.1 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:69583137 G>A maps to NM_021800.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:132182589 A>G maps to NM_015268.3 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:132211374 C>T maps to NM_015268.3 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:132241715 T>C maps to NM_015268.3 D1906D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:132169489 G>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:132203455 G>T maps to NM_015268.3 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:132172953 C>A maps to NM_015268.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr12:56221154 G>A maps to NM_032364.5 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:49743485 G>T maps to NM_024902.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:25170607 G>C maps to NM_016544.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:65858249 C>G maps to ENST00000371069 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr17:40135655 T>C did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:153631372 G>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:153633250 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:84880304 C>T maps to NM_021233.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:230312224 C>A maps to NM_139072.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:230453204 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:10893690 C>T maps to NM_001005361.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:10908187 C>T maps to NM_001005361.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:10913019 C>T maps to NM_001005361.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr19:10904483 C>T maps to NM_001005361.2 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:172050970 G>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:172011203 C>T maps to ENST00000359070 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:171810834 G>T maps to ENST00000359070 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:101656025 G>A maps to ENST00000342239 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr10:101716837 C>A maps to ENST00000342239 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr10:101636940 G>A maps to ENST00000342239 P1591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:25467479 G>A maps to NM_175629.1 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:25523040 C>A maps to NM_175629.1 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:25497890 C>A maps to NM_175629.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr20:31394016 A>G maps to NM_006892.3 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr21:45679432 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr10:98078222 G>A maps to NM_004088.3 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:94342029 T>A maps to NM_014597.4 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr10:129046348 T>C maps to ENST00000398025 F1020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr10:129237452 C>T maps to ENST00000398025 S1786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:225702548 C>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:225721668 C>T maps to NM_014689.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:225729637 G>C maps to NM_014689.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr2:225717813 A>G maps to NM_014689.2 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:117749583 G>C did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:117814527 A>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:117731470 C>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:117773510 G>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:117700046 A>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:117731507 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:117749671 A>C did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:117764394 G>C did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:117743288 T>A did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr23:117788714 G>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:117815707 G>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:117777530 G>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:117809914 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:169188552 C>T maps to NM_004946.2 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr5:169423110 C>T maps to NM_004946.2 N1005N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:169494608 C>A maps to NM_004946.2 T1521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr5:169483699 C>A maps to NM_004946.2 S1436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr5:169111315 C>T maps to NM_004946.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr5:169144477 T>C maps to NM_004946.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr5:169081482 G>T maps to NM_004946.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr5:169507177 G>A maps to NM_004946.2 K1726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:51196712 C>T maps to NM_004947.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr3:51400046 G>C maps to NM_004947.4 L1745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:111638558 C>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:111430511 C>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:111509671 G>T maps to ENST00000428084 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:111462505 G>A maps to ENST00000428084 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr8:25250370 G>A maps to NM_024940.6 K1500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:11362851 G>A maps to ENST00000319867 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:11326503 G>A maps to ENST00000319867 R1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr19:11361675 T>G maps to ENST00000319867 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:11338083 C>A maps to ENST00000319867 G962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:11332605 C>T maps to ENST00000319867 V1157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:62943400 G>A maps to ENST00000371140 T1868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr1:63100503 C>A maps to ENST00000371140 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:63090928 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:62960017 T>G maps to ENST00000371140 A1715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:439279 C>T maps to NM_203447.3 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr9:340231 G>C maps to NM_203447.3 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr9:464217 A>T maps to NM_203447.3 *2100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr13:99489834 C>A maps to ENST00000428223 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:74783970 G>T maps to NM_001381.3 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr8:21769829 G>A maps to NM_003974.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:176931331 G>A maps to NM_024872.2 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr5:176931127 C>T maps to NM_024872.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr5:176931493 C>A maps to NM_024872.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr20:53205080 T>C maps to NM_018431.3 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr9:131708256 G>A maps to NM_014908.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:131846977 G>T maps to NM_020438.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:83861600 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr21:37581180 G>T maps to NM_005128.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr21:37618876 C>G maps to NM_005128.2 S1533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr21:37649358 G>T maps to NM_005128.2 P1891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:2191144 C>G maps to ENST00000221482 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:2185886 C>A maps to ENST00000221482 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:118971748 A>G maps to NM_001382.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:103360568 C>T maps to NM_015448.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr6:30919762 G>A maps to NM_080870.3 T1174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr16:89702986 C>T maps to NM_004413.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:68026024 G>A maps to NM_022355.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr16:68012233 G>A maps to NM_022357.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:65107888 G>A maps to NM_006268.3 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:65113401 C>G maps to NM_006268.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr14:73238546 T>G maps to NM_012074.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr14:73238590 G>A maps to NM_012074.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:44437887 C>T maps to NM_001384.4 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr9:130699796 C>A maps to ENST00000373110 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:116572494 G>A maps to NM_020868.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr2:116548754 G>T maps to NM_020868.3 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:115200384 C>T maps to NM_020868.3 H10H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:116594281 G>A maps to NM_020868.3 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:116534782 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr2:116593752 A>T maps to NM_020868.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:116548747 C>T maps to NM_020868.3 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:66254030 C>T maps to NM_005700.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr2:162902047 G>T maps to NM_001935.3 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:162890070 A>G maps to NM_001935.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr2:162865768 T>C maps to NM_001935.3 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:162881448 C>A maps to NM_001935.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:162851469 C>T did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:162929975 C>A maps to NM_001935.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:162865780 C>A maps to NM_001935.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr7:154595608 C>T maps to NM_130797.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr7:154561256 C>T maps to NM_130797.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr7:154587593 G>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr7:154263964 T>C maps to NM_130797.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:109033355 C>A did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:109026973 G>T maps to NM_138815.3 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:109023452 C>A maps to NM_138815.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:109026912 A>C maps to NM_138815.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:109028124 G>T maps to NM_138815.3 C78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:7868816 G>A maps to NM_199286.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:7869564 G>A maps to NM_199286.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:109052820 G>T maps to NM_018189.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr3:109052760 G>T maps to NM_018189.3 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr3:109049431 C>T maps to NM_018189.3 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:109049618 G>C maps to NM_018189.3 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr19:54137818 C>A maps to NM_001012728.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:168698285 G>T maps to NM_001937.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:168698148 C>G maps to NM_001937.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr7:34971193 T>A maps to NM_015283.1 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:63974448 G>T maps to NM_173812.4 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:63954357 T>C maps to NM_173812.4 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr12:64011104 A>C maps to NM_173812.4 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:63987865 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:32899170 C>T maps to NM_001172774.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:32949040 T>C maps to NM_001172774.1 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:32968457 G>C maps to NM_001172774.1 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:32955671 G>T maps to NM_001172774.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:95751681 A>T maps to NM_181787.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:97547897 A>G maps to NM_000110.3 D965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:98039314 C>G did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:98165060 G>A maps to NM_000110.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:97547957 C>A maps to NM_000110.3 V945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr8:105405188 A>C maps to NM_001385.2 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:105405019 G>A maps to NM_001385.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:146778758 G>T maps to NM_001197294.1 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:134006185 C>T maps to NM_006426.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:134006221 G>T maps to NM_006426.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr10:134012416 C>T maps to NM_006426.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:74747069 C>G maps to NM_133637.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:111663189 G>C maps to NM_178454.4 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:174869481 C>A maps to NM_000794.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:113890719 G>A maps to NM_000796.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:113890803 G>A maps to NM_000796.3 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:113847631 G>A maps to NM_000796.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:9784693 C>T maps to NM_000798.4 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr4:9784720 C>T maps to NM_000798.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr4:9783787 C>T maps to NM_000798.4 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr4:9784819 C>T maps to NM_000798.4 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:100490872 G>T did not map to a codon.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr23:100494029 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:100509888 C>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:100505426 T>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:100497459 G>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:100510220 G>T did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:100503556 G>C did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr18:28659822 T>C maps to ENST00000438199 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr18:28666568 G>T maps to ENST00000438199 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr18:28598039 T>A maps to NM_001941.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr18:28586894 C>A maps to NM_001941.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr21:41725407 G>A maps to NM_001389.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr21:41741059 C>G maps to NM_001389.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr21:41414426 C>A maps to NM_001389.3 E1853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr21:42064817 G>T maps to NM_001389.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr21:41385158 C>T maps to NM_001389.3 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr21:41385158 C>T maps to NM_001389.3 P1947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:41385098 G>T maps to NM_001389.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:117306408 G>A maps to NM_020693.2 L1669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:117351886 A>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:117310039 C>G maps to NM_020693.2 T1422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:117303184 C>A maps to NM_020693.2 E1748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr11:117335862 C>G maps to NM_020693.2 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr11:117307859 G>A maps to NM_020693.2 F1626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:117314734 C>T maps to NM_020693.2 T1303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:117351982 G>C maps to NM_020693.2 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:117647596 G>A maps to NM_020693.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:116758234 G>A maps to NM_013352.2 E868E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr6:116756864 A>T maps to NM_013352.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr18:65180603 G>A maps to NM_032160.2 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr18:65180601 C>T maps to NM_032160.2 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr18:28918391 C>A maps to NM_001942.2 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr18:28934435 A>T maps to NM_001942.2 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr18:29126517 C>T maps to NM_001943.3 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr18:29056144 C>A maps to NM_001944.2 G974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr18:28992991 G>T maps to NM_001134453.1 E872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr18:28986103 G>T maps to NM_001134453.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr18:28989766 C>T maps to NM_177986.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr6:7584769 C>A maps to NM_004415.2 T2425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr6:7572249 A>T maps to NM_004415.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:7569564 C>T maps to NM_004415.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr6:7571677 A>G maps to NM_004415.2 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr4:88535379 T>C maps to NM_014208.3 N522N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr4:88532088 G>A maps to NM_014208.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:56462638 C>A maps to ENST00000361203 G3821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:56334982 A>C maps to ENST00000361203 L7235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:56504518 A>T maps to ENST00000361203 L680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:56382352 C>A maps to ENST00000361203 L5854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr6:56494055 A>T maps to ENST00000361203 I1278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:56458655 C>T maps to ENST00000361203 Q3966Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:56394533 T>C maps to ENST00000361203 L5558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:17581498 C>T maps to NM_006870.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:205116793 C>T maps to NM_015375.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:205116780 A>G maps to NM_015375.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr18:32418762 C>A maps to NM_001390.4 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr18:32462134 G>C maps to NM_001390.4 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr12:113531398 C>G maps to NM_004416.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:76111996 C>T maps to NM_020892.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:76126660 G>T maps to NM_020892.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr3:122288681 C>T maps to NM_138287.3 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr3:122284829 G>C maps to NM_138287.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr3:122287796 G>A maps to NM_138287.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr3:122287848 C>T maps to NM_138287.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:58972186 C>G maps to NM_015177.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr15:45427449 C>T maps to NM_175940.1 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:45398788 T>A maps to NM_014080.4 K628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:45401779 C>A maps to NM_014080.4 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:45402881 G>A maps to NM_014080.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:45409294 G>A maps to NM_207581.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr15:45408421 C>A maps to NM_207581.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:76818228 G>T maps to NM_001003892.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:5785252 G>A maps to NM_020175.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:221913077 C>T maps to NM_007207.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr2:73993666 G>A maps to NM_003584.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr17:35872856 C>T maps to NM_007026.2 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr22:31059939 G>A maps to NM_152511.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:183943828 T>C maps to NM_080876.3 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:96810553 C>A maps to NM_004418.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:44703483 G>T did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:44703623 C>T did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr6:335142 G>T maps to ENST00000457386 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:167095387 C>T maps to NM_001080426.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:167097049 G>A maps to NM_001080426.1 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:167095786 G>T maps to NM_001080426.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:167097662 G>T maps to NM_001080426.1 G1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr1:167088692 G>A maps to NM_001080426.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:167097463 C>A maps to NM_001080426.1 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:167086652 C>T maps to NM_001080426.1 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:167086706 G>C maps to NM_001080426.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:167096614 G>C maps to NM_001080426.1 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:52085121 C>T maps to NM_001947.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:152915068 C>A did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr23:152915068 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:1274965 T>C maps to ENST00000378888 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr17:7130725 G>A maps to NM_004422.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr17:7133692 C>G maps to NM_004422.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr3:183887878 G>A maps to NM_004423.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:102442055 C>T maps to NM_001376.4 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:102476636 C>T maps to NM_001376.4 S2082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr14:102474666 C>A maps to NM_001376.4 Y1990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr14:102460519 G>C did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr14:102516142 G>A maps to NM_001376.4 L4536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:102489100 G>T maps to NM_001376.4 E2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:102472280 T>C maps to NM_001376.4 I1830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr14:102484925 C>A maps to NM_001376.4 A2772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr14:102507986 C>T maps to NM_001376.4 H4006H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:102510220 G>T maps to NM_001376.4 E4175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:102478378 C>T maps to NM_001376.4 D2262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr14:102498738 C>T maps to NM_001376.4 I3338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:102515001 G>T maps to NM_001376.4 V4456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:102505345 C>T maps to NM_001376.4 Q3739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr14:102499790 C>T maps to NM_001376.4 I3461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr14:102476339 G>T maps to NM_001376.4 R2046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr14:102471150 G>A maps to NM_001376.4 W1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:95606828 G>T maps to NM_004411.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr7:95499245 G>T maps to NM_004411.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr7:95709709 C>A maps to NM_004411.4 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:103029720 C>G maps to NM_001080463.1 S1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr2:44023054 G>T maps to NM_001193464.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr2:44032357 C>T maps to NM_001193464.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:37699872 G>T did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr21:38862489 C>G maps to NM_001396.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:40316474 T>A maps to NM_004714.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:68051496 G>T maps to NM_006482.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:68051553 G>A maps to NM_006482.2 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:71709006 A>T did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr2:71886093 C>G maps to NM_001130987.1 P1614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:71740930 G>T maps to NM_001130987.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:71795348 G>C maps to NM_001130987.1 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:71780186 C>G maps to NM_001130987.1 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:71883309 G>T maps to NM_001130987.1 E1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:71747931 C>T maps to NM_001130987.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr2:71891466 C>T maps to NM_001130987.1 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:71753402 C>G maps to NM_001130987.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr2:71740978 C>T maps to NM_001130987.1 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr2:207527888 C>T maps to NM_001093730.1 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr15:55790003 A>G maps to NM_130810.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr13:96293632 C>T maps to NM_198968.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr13:96277156 C>T maps to NM_198968.2 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:137816614 C>T maps to NM_173543.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr3:108363258 C>T maps to NM_014648.3 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:108409674 G>A maps to NM_014648.3 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr11:19246330 G>A maps to NM_024680.2 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr16:2282274 C>G maps to NM_004424.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:121591525 A>G maps to NM_018456.4 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:35002667 C>A maps to NM_018453.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:158223415 G>A maps to NM_024007.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr5:158141189 C>A maps to NM_024007.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:25766019 T>A maps to NM_022659.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:25744280 G>A maps to NM_022659.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr8:25745432 G>A maps to NM_022659.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:25897592 T>A maps to NM_022659.2 K145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:25899691 G>A maps to NM_022659.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr10:131757214 G>C maps to ENST00000355311 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr10:131761759 G>A maps to ENST00000355311 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:48386662 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr13:50265551 A>G maps to NM_032565.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr10:74899086 G>A maps to NM_001135752.1 H500H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr1:21564677 C>A maps to NM_001397.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:21571586 G>A maps to NM_001397.2 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr3:183995719 C>T maps to NM_014693.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:184002857 G>A maps to NM_014693.3 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:184003352 G>T maps to NM_014693.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr3:184005695 C>T maps to NM_014693.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr2:233344864 A>G maps to NM_004826.2 *776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:39307162 C>A maps to NM_001398.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:127637623 G>A maps to NM_001139510.1 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr9:95264874 G>C maps to NM_001393.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:11624937 G>C maps to NM_016581.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:172482144 T>G maps to ENST00000392692 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr3:172491778 C>A maps to ENST00000392692 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr3:172537960 C>T maps to ENST00000392692 V893V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr23:65824982 C>A did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:109513382 G>A maps to ENST00000376651 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:236590722 C>A maps to NM_145861.2 C64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:236645624 G>T maps to NM_145861.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:67917563 C>T maps to NM_014329.3 Q1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:67916220 C>G maps to NM_014329.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:5243500 C>T maps to NM_014674.2 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr20:33703373 T>A maps to NM_018217.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr5:83360517 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:148441067 C>T maps to NM_001957.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:148453688 C>T maps to NM_001957.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr13:78492547 C>T maps to ENST00000377211 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr13:78474024 A>T maps to ENST00000377211 L478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr13:78492261 C>A maps to ENST00000377211 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr2:207026082 A>T maps to NM_021121.3 K73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:207027297 C>T maps to NM_021121.3 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr11:62339044 G>A maps to ENST00000378019 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:22262525 C>T maps to NM_013302.3 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr16:22261998 G>T maps to NM_013302.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr16:22291591 G>T maps to NM_013302.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:127965811 C>G maps to NM_021937.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:128060230 G>A maps to NM_021937.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:49641663 T>C maps to NM_024593.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr12:3788199 G>C maps to NM_001144958.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr12:3782627 C>A maps to NM_001144958.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr12:3763444 G>A maps to NM_001144958.1 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr17:28296328 G>A maps to NM_198529.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:28380315 G>A maps to NM_198529.3 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr22:44028020 C>T maps to NM_022785.3 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr22:44031097 T>C did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:64034099 C>T maps to NM_032437.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:56097911 G>A maps to NM_001039349.1 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:65638667 G>A maps to NM_016938.3 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr11:65634505 C>T maps to NM_016938.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr13:22084200 G>A maps to NM_152726.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr13:22140934 C>G did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr8:16962000 G>A did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:19938193 G>A maps to NM_144715.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:19956849 T>C maps to NM_144715.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:44091789 G>A did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:44109543 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:44120490 A>G did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:44101368 G>A did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:233546383 C>G maps to NM_025202.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:233527617 G>T maps to NM_025202.3 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:68060179 G>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:68060193 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:68059885 G>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr13:107145563 T>A maps to NM_004093.2 K276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr13:107187249 T>C maps to NM_004093.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr13:107165087 C>A maps to NM_004093.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:7612579 C>T maps to NM_001406.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:133014040 G>A maps to NM_015137.3 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:42937900 C>A maps to NM_004247.3 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:42931685 G>A maps to NM_004247.3 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr4:110915913 G>A maps to NM_001963.4 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr4:110864591 G>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:13651196 T>G did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:13645159 T>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:32134486 C>T maps to NM_030652.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:38458494 A>C maps to ENST00000354891 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:38338835 C>T maps to ENST00000354891 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr5:38435306 G>T maps to ENST00000354891 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr5:38350604 G>A maps to ENST00000354891 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr5:38352407 C>T maps to ENST00000354891 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:55220236 A>G did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr7:55231500 C>T maps to NM_005228.3 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr14:34400376 G>C maps to NM_022073.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr8:22548417 G>T maps to NM_004430.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:73519556 A>G maps to NM_001965.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:63101541 C>T maps to NM_015252.3 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:63101594 C>T maps to NM_015252.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:63176203 G>A maps to NM_015252.3 K776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:63092064 C>G maps to NM_015252.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64645801 G>A maps to NM_006795.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr2:31472299 G>A maps to NM_014600.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:34680083 G>C maps to NM_012153.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:184910688 G>A maps to NM_001966.3 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:184953215 T>C maps to NM_001966.3 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr9:140637892 G>T maps to NM_024757.4 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:140712551 C>T maps to NM_024757.4 R1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:31864516 G>T maps to ENST00000395728 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:31854776 G>A maps to ENST00000395728 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:125449999 G>T maps to ENST00000278903 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:65767581 C>T maps to NM_032325.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr3:150301009 G>A maps to NM_032025.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:6077057 C>G maps to NM_014413.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:6089540 A>T did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr2:88888333 G>T maps to NM_004836.5 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:40247943 C>A maps to NM_001013703.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr14:75471539 C>G maps to NM_014239.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:45347341 T>A maps to NM_020365.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr1:45444121 C>A maps to NM_020365.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:27591275 G>A maps to NM_172195.3 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:183858307 C>T maps to NM_003907.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:183859719 C>T maps to NM_003907.2 N388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:141583032 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:141559240 G>C maps to NM_012154.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:141582931 G>A maps to NM_012154.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:36439030 C>T maps to NM_024852.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:36506012 C>A maps to NM_024852.2 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr14:67831576 G>A maps to NM_004094.4 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:24078261 C>T did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr10:120810777 G>T maps to NM_003750.2 S751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr10:120796676 G>A maps to NM_003750.2 D1291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr10:120801830 C>A maps to NM_003750.2 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr10:120795712 T>A maps to NM_003750.2 R1329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr10:120802058 G>A maps to NM_003750.2 N991N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:120797900 G>T maps to NM_003750.2 R1193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:2402713 G>T maps to ENST00000314800 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr22:36907703 G>A maps to NM_003753.3 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr8:109226864 G>A maps to NM_001568.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:8016064 G>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr8:117669518 T>C maps to ENST00000411422 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr19:39114782 C>T maps to NM_013234.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:38273862 C>T maps to ENST00000262832 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:186504959 C>A maps to ENST00000440191 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:99823127 G>A maps to NM_001130679.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr3:71745663 C>A maps to NM_001134651.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr8:37914608 C>T maps to NM_004095.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:31864272 G>A maps to NM_019843.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr22:31835937 A>G maps to NM_019843.3 D962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr22:31867894 G>C maps to NM_019843.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr3:184038428 A>T maps to NM_001194947.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:184041674 C>G maps to NM_001194947.1 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:184045479 C>A maps to NM_001194947.1 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:10821166 T>C maps to ENST00000429377 K825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:10827515 G>A maps to ENST00000429377 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:10825568 G>A maps to ENST00000429377 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:21144031 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:21177915 G>T maps to NM_001198801.1 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr14:103805110 G>T maps to NM_183004.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr14:103802452 G>T maps to NM_183004.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:12897090 C>T maps to NM_018127.6 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:855688 G>A maps to NM_001972.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:8045965 C>A did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr19:8032654 C>A maps to ENST00000351593 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr9:23701420 G>A maps to ENST00000359598 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr13:41533077 G>A maps to NM_172373.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:201983143 G>A maps to NM_004433.4 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:201980362 C>T maps to NM_004433.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:129201403 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:129203532 G>C did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:129205106 G>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:129205332 C>G did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:129203603 C>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr22:37769708 C>A maps to NM_052906.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:47496453 C>T did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:96617397 G>A maps to NM_005230.2 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:95224672 C>A maps to NM_012081.5 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr5:95224660 T>A maps to NM_012081.5 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:44066937 C>A maps to NM_025165.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:37264596 C>A maps to NM_014800.9 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr7:37136260 G>T maps to NM_014800.9 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr20:44997541 A>G maps to ENST00000439931 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:107501161 C>T maps to NM_018712.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:85598246 C>A maps to NM_001135023.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr7:73462839 C>A maps to ENST00000358929 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr7:73461083 C>G maps to ENST00000358929 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr10:103987390 C>G maps to NM_152310.1 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr10:103987487 C>G maps to NM_152310.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:60062458 T>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr18:33722804 A>T maps to ENST00000442325 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:27989845 C>T maps to NM_018091.5 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr11:31648665 C>A maps to ENST00000395934 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr19:48517488 C>A maps to NM_022142.4 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr1:79403540 G>A maps to NM_022159.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:79387436 C>T maps to NM_022159.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:79403965 T>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:79385866 C>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:79383531 A>T maps to NM_022159.3 Y555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:79383617 C>A maps to NM_022159.3 G527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:153609142 G>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:153609539 G>T did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr17:48456521 G>A maps to NM_001166131.1 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr22:29628306 G>T maps to NM_133455.2 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:27305105 C>T maps to NM_007046.3 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:2891882 C>G maps to NM_032048.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr18:2909705 C>T maps to NM_032048.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr18:2892172 C>A maps to NM_032048.2 S683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr20:39990767 G>A maps to NM_052846.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr20:39991676 G>A maps to NM_052846.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr14:100375747 G>T maps to NM_001008707.1 G410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr14:100331947 G>T maps to NM_001008707.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr19:46127983 C>T maps to NM_001193268.1 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:62378412 C>T maps to ENST00000278845 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr2:42511824 C>T maps to NM_019063.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:42483654 C>T maps to NM_019063.3 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:89181376 G>A maps to ENST00000380664 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr14:89123747 G>A maps to ENST00000380664 Q1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr14:89181370 A>G maps to ENST00000380664 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr16:10631854 G>A maps to NM_001424.4 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr19:6919664 G>T maps to ENST00000381407 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:6921839 C>A maps to ENST00000381407 C581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:14740934 G>T maps to NM_032571.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:73160998 G>A maps to NM_004097.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:119604347 G>T maps to NM_001426.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr7:155255318 C>G maps to NM_001427.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr4:71509218 C>A maps to NM_031889.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr4:71509750 C>T maps to NM_031889.2 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:71508516 G>A maps to NM_031889.2 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:73932187 C>T maps to NM_003633.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:94862073 A>G maps to NM_015036.2 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:77082340 A>G maps to NM_001042573.1 E714E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:4858861 C>A maps to NM_053013.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr18:706488 C>A maps to ENST00000319815 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:129804101 C>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:129801609 G>C did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:129799637 G>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:129837177 T>C did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:129813617 C>A did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:129790625 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:129759345 C>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr4:111471003 T>C maps to NM_001977.3 Y821Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr4:111397797 C>T maps to NM_001977.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr4:111463935 G>T maps to NM_001977.3 G613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr4:111482594 G>T maps to NM_001977.3 G919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:132179887 G>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:132206131 C>A maps to NM_006208.2 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:132171155 G>T maps to NM_006208.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:132203588 G>T maps to NM_006208.2 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:120581496 G>A maps to NM_006209.3 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:120592359 T>C maps to NM_006209.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:120594756 G>A maps to NM_006209.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:120569784 C>T maps to NM_006209.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr6:132004192 G>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:132014755 G>T maps to NM_005021.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr6:132014690 C>T maps to NM_005021.3 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr6:132014719 C>A maps to NM_005021.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr6:131973775 T>C maps to NM_005021.3 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:46107760 C>T maps to NM_014936.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:46111175 G>A maps to NM_014936.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr6:46107440 C>T maps to NM_014936.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr6:46108001 G>T maps to NM_014936.4 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr6:46135372 T>A maps to NM_021572.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:77704930 G>C maps to NM_178543.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr17:77705075 C>T maps to NM_178543.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr8:23305379 G>A maps to NM_004901.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:74443725 C>G did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:25193990 A>T maps to NM_001247.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr20:25203567 T>C maps to NM_001247.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:110355664 C>A maps to NM_020189.5 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:41572363 C>T maps to NM_001429.3 L1631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:41574203 C>T maps to NM_001429.3 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr22:41565504 A>G did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr12:132551416 C>T maps to ENST00000333577 S2920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:132537711 G>A maps to ENST00000333577 P2508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr12:132445646 C>G maps to ENST00000333577 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:132549311 C>T maps to ENST00000333577 Q2848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:132562019 C>T maps to ENST00000333577 T3094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr12:132508340 A>T maps to ENST00000333577 I1606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr12:132516565 C>A maps to ENST00000333577 T1977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:46607559 C>T maps to NM_001430.4 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:34773051 C>T maps to NM_012156.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr6:131222121 T>A maps to NM_001431.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:131277399 G>T maps to NM_001431.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:131186729 T>C maps to NM_001431.3 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:131276357 G>A maps to NM_001431.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr6:131216112 C>T maps to NM_001431.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr6:131215518 T>C maps to NM_001431.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr18:5438110 T>A did not map to a codon.
Alternatively spliced codon TCGA-22-5492-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr18:5419874 C>T maps to NM_012307.2 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr18:5434019 C>A maps to NM_012307.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr18:5416378 T>A did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr18:5424261 T>A maps to NM_012307.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr18:5428400 G>T maps to NM_012307.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr18:5394783 A>C maps to NM_012307.2 A1054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr18:5428394 G>A maps to NM_012307.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr18:5395707 T>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:111504717 C>T maps to NM_022140.3 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr9:111945035 A>G maps to NM_019114.3 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr9:112030677 C>T maps to NM_019114.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:120918469 G>T maps to NM_020909.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr15:43494123 G>A maps to NM_000119.2 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr8:21937754 G>C maps to ENST00000265800 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr2:47612312 C>G maps to ENST00000426238 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:143096483 C>T maps to NM_005232.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr7:143096795 C>T maps to NM_005232.4 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:38227318 G>T maps to NM_001099439.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:38187349 C>A maps to NM_001099439.1 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:38197176 G>A maps to NM_001099439.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:16456842 G>T maps to NM_004431.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:89391076 C>T maps to NM_005233.5 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr3:89521679 G>A maps to NM_005233.5 W919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr3:89391047 C>T maps to NM_005233.5 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:89390084 C>T maps to NM_005233.5 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:89498460 G>T maps to NM_005233.5 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:89528544 A>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr3:89521661 C>T maps to NM_005233.5 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:89448475 A>G maps to NM_005233.5 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr3:89456488 C>A maps to NM_005233.5 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:222428691 C>A maps to NM_004438.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr2:222428481 A>T maps to NM_004438.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:66197846 C>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:66467452 G>T maps to NM_004439.5 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr4:66189897 C>T maps to NM_004439.5 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:66213855 G>T maps to NM_004439.5 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr4:66270099 G>A maps to NM_004439.5 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:66280000 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr4:66535394 G>T maps to NM_004439.5 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:66467467 C>A maps to NM_004439.5 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr3:97454767 G>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:96706478 C>A maps to NM_001080448.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:97194253 C>A maps to NM_001080448.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr3:96533583 G>T maps to NM_001080448.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr3:97454853 G>A maps to NM_001080448.2 W1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:97356889 G>C maps to NM_001080448.2 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:97251211 A>T maps to NM_001080448.2 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr6:93967178 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:93969135 A>T maps to NM_004440.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:22924241 C>T maps to NM_020526.3 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:22921765 G>T maps to NM_020526.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:22902720 C>T maps to NM_020526.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:22927416 C>A maps to NM_020526.3 Y855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr1:22922655 G>A maps to NM_020526.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:134873024 C>G maps to NM_004441.4 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr3:134898765 G>T maps to NM_004441.4 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:134825428 A>T maps to NM_004441.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr3:134670775 A>G maps to NM_004441.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:134851891 G>C did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:134881014 G>T maps to NM_004441.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr3:134670814 G>A maps to NM_004441.4 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:134960003 T>C maps to NM_004441.4 P787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr3:134967228 C>A maps to NM_004441.4 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:23191523 C>T maps to ENST00000400191 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:184294843 G>T maps to NM_004443.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:184294687 C>T maps to NM_004443.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:184294817 C>A maps to NM_004443.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:100405040 G>A maps to NM_004444.4 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:100404040 C>T did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:100403229 C>T maps to NM_004444.4 W857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:100421298 G>A maps to NM_004444.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr7:142561729 G>T maps to NM_004445.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr7:142568387 C>T maps to NM_004445.3 F969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:142562439 A>T maps to NM_004445.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:226016447 C>G maps to NM_001136018.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr8:27361173 C>T maps to ENST00000458037 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:15338337 G>A maps to NM_001142886.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:92498144 C>T maps to NM_173567.4 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr1:92528791 G>C maps to NM_173567.4 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr3:37034358 C>A maps to NM_014805.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr3:37032747 T>C maps to NM_014805.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr3:37033874 G>A maps to NM_014805.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr7:100319235 C>G maps to NM_000799.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:100320734 C>A maps to NM_000799.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:11489064 C>T maps to NM_000121.3 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:144940425 C>T maps to NM_031308.1 R2332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr8:144946302 G>T maps to NM_031308.1 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:144940677 G>A maps to NM_031308.1 A2248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr8:144943647 G>C maps to NM_031308.1 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr8:144942408 G>C maps to NM_031308.1 L1671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr8:144941085 C>T maps to NM_031308.1 V2112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr8:144943083 G>T maps to NM_031308.1 T1446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr8:144943413 G>C maps to NM_031308.1 L1336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:220178659 T>A maps to NM_004446.2 K665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:51946953 G>C maps to NM_001981.2 Y22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:16514639 C>T maps to ENST00000455140 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:15813566 A>G maps to NM_004447.5 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:110302412 C>A maps to NM_139053.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr13:43462601 T>C maps to NM_001002264.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:26597906 G>T did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:56270462 G>A maps to NM_000502.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:56270815 A>G maps to NM_000502.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:27186252 G>T maps to NM_005702.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:48687602 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:48687892 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:48688085 C>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr17:37866732 C>T maps to NM_004448.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:65342182 C>A maps to ENST00000506030 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:212566847 G>A maps to NM_005235.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:212566891 C>A did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:212989623 A>T maps to NM_005235.2 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:212483997 A>C maps to NM_005235.2 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr2:212285213 G>A maps to NM_005235.2 N1029N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr12:1192739 G>A maps to NM_178040.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:1480997 G>A did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr3:55922475 C>A maps to ENST00000460849 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:45856556 G>C maps to NM_000400.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr19:45864869 C>T maps to NM_000400.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:128030505 C>A maps to NM_000122.1 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr2:128030446 T>A maps to NM_000122.1 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:14026041 G>A maps to NM_005236.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr13:103504583 C>T maps to NM_000123.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr13:103528078 G>T maps to NM_000123.2 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:50678600 T>C maps to NM_000124.2 T1135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:71427656 G>T did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:71425952 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:71426085 T>C did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:71425038 G>C did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:60194176 C>A maps to NM_000082.3 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:42752688 G>C maps to NM_006494.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr19:42752781 G>A maps to NM_006494.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:172351072 G>T maps to NM_001031711.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr8:8873830 G>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:44687310 G>A maps to NM_024066.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:23716313 C>A maps to NM_033266.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:236399130 G>A maps to NM_019891.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:236396137 G>A maps to NM_019891.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:236388416 C>A maps to NM_019891.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr12:15068527 T>C maps to NM_152321.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:15073865 C>T maps to NM_152321.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:124623855 C>A maps to NM_138961.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:19116017 C>T maps to NM_052911.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr18:19154257 T>A maps to NM_052911.2 K183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr8:27657188 G>T maps to NM_001017420.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr8:27646494 G>A maps to NM_001017420.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr20:13756703 C>A maps to NM_016649.3 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:53677226 G>A maps to NM_012291.4 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:53682973 C>T maps to NM_012291.4 F1603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr12:53663319 G>T maps to NM_012291.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:53671295 G>T maps to NM_012291.4 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:6512047 C>T maps to NM_031475.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr6:152265431 G>T maps to NM_001122741.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:152415691 C>A maps to NM_001122741.1 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:64083326 C>A maps to NM_004451.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:64074791 C>G maps to NM_004451.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr14:76928996 G>A maps to NM_004452.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr14:76949082 C>A maps to NM_004452.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:216850646 C>A maps to NM_001438.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:216741399 G>T maps to NM_001438.2 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:216850833 C>T did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:103495291 A>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:103495395 G>A did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr12:56522357 C>T maps to NM_001184796.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:138178091 C>T maps to NM_031913.3 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr3:138183262 C>G maps to NM_031913.3 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr3:138174128 C>T maps to NM_031913.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr2:67630365 A>T maps to NM_019002.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:76566835 C>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr15:76588073 G>T maps to NM_000126.3 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:44011034 G>A maps to NM_014297.3 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:22812019 T>G maps to NM_018638.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:128359269 G>A maps to NM_001143820.1 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr11:128360394 G>A maps to NM_001143820.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:128360361 C>T maps to NM_001143820.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:13971313 C>T maps to NM_004956.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr7:13949272 G>C maps to NM_004956.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:36135684 C>T maps to ENST00000222279 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:157104019 C>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:157062599 C>A maps to NM_001004341.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr17:41610574 A>G maps to NM_001079675.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:185766535 G>A maps to NM_004454.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr12:12037424 C>T maps to NM_001987.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr6:36336810 G>A maps to NM_016135.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:5733381 G>A maps to NM_153717.2 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:5664931 G>A maps to NM_147127.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:5620294 C>A maps to NM_147127.4 R872R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr4:5699344 C>A maps to NM_147127.4 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:5699317 A>G did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:93160929 A>C maps to NM_005665.4 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:92979245 C>A maps to NM_005665.4 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:92979448 C>A maps to NM_005665.4 G733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr19:7914139 A>G did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:74013979 G>C maps to NM_001988.2 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr17:74023264 C>A maps to NM_001988.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:27282756 G>T maps to NM_001989.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:176948393 G>T maps to NM_001080458.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr15:41476287 T>C maps to NM_152596.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr9:140243630 G>A maps to NM_017820.3 H587H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:140245773 C>T maps to NM_017820.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:242045215 A>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:242024770 A>G maps to NM_006027.4 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:242042218 T>C maps to NM_006027.4 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:242021896 G>C maps to NM_006027.4 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr1:242035335 G>T maps to NM_006027.4 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:56737264 A>G did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr4:56738081 C>T maps to NM_018261.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:486757 C>A maps to NM_018303.4 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr6:562783 T>G maps to NM_018303.4 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:633007 G>T maps to NM_018303.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:133580389 G>A maps to NM_021807.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr7:132973848 T>C maps to NM_021807.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:57686089 A>T maps to ENST00000340918 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:57698408 C>A maps to ENST00000340918 L323L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-60-2715-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:72719550 C>A maps to NM_015189.1 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:72968456 C>A maps to NM_015189.1 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:38537941 T>A maps to NM_005107.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:11137692 C>A maps to NM_001001998.1 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:108385420 G>A maps to NM_015065.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:108384541 C>A maps to NM_015065.2 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr11:108382900 T>C maps to NM_015065.2 R1111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr11:108382993 T>C maps to NM_015065.2 E1080E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:108380314 G>T maps to NM_015065.2 T1973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:108382261 G>C maps to NM_015065.2 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:108385054 T>A maps to NM_015065.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:108398895 T>G maps to NM_015065.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:119122649 G>A maps to NM_000127.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:44146494 C>T maps to NM_000401.3 C333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:26349715 C>A maps to NM_004455.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:26360263 C>T maps to NM_004455.2 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:101339554 G>A maps to NM_001439.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:45633652 G>A maps to ENST00000360649 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:133802601 A>T maps to ENST00000452339 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:133783574 C>A maps to ENST00000452339 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr6:133703558 T>A maps to ENST00000452339 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:133783757 G>C did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:66044901 A>T maps to ENST00000370616 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:66112498 C>A did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr6:66044996 G>A maps to ENST00000370616 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr6:66200498 C>A maps to ENST00000370616 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr6:66205242 C>A maps to ENST00000370616 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr17:40861922 G>T maps to ENST00000264646 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr17:40858078 C>T maps to ENST00000264646 W598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:148511203 G>A maps to NM_004456.3 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:148512010 G>C maps to NM_004456.3 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr7:148515179 G>C maps to NM_004456.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:148516728 G>A maps to NM_004456.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:148506221 C>T maps to NM_004456.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr13:113798357 C>G maps to NM_000504.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr13:113803803 G>A maps to NM_000504.3 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr4:187201391 C>A maps to NM_000128.3 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:160990842 G>C maps to NM_016946.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr5:176833015 G>A maps to NM_000505.3 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr6:6224961 G>T maps to NM_000129.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:6318806 C>A maps to NM_000129.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:6182371 G>T maps to NM_000129.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:6182227 G>A maps to NM_000129.3 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:197021953 A>G maps to NM_001994.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr1:197026479 C>T maps to NM_001994.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:17001362 C>G maps to NM_003950.2 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:169511511 G>T maps to ENST00000367796 S944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:169510280 G>T maps to ENST00000367796 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:169555504 G>A maps to ENST00000367796 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:169555540 C>A maps to ENST00000367796 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr13:113768230 C>T maps to NM_000131.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:154185446 C>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:154182253 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:154134723 T>C did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:154157065 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:154157609 G>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:154182311 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:154182255 T>A did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:154158966 T>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:154185348 A>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:154250706 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:154159453 C>G did not map to a codon.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr23:154189423 G>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:138630562 T>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:138630607 G>A did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr23:138619202 G>C did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:138643728 T>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:138644098 G>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:138623347 G>T did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr23:138643920 C>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:138619260 G>C did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:46874150 C>G maps to NM_001441.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:57358225 T>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:57313334 G>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr23:57515354 G>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:57313305 G>C did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:82441722 T>A maps to NM_001105281.1 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr8:82196795 A>G maps to NM_001444.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr8:82195649 T>C maps to NM_001444.1 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:159661867 C>T maps to NM_001040442.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr11:70049645 C>A maps to NM_003824.3 C27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:70049750 C>T maps to NM_003824.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:61645000 C>A maps to NM_021727.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72888658 G>A maps to ENST00000310226 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr15:80469897 G>T maps to NM_000137.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:80465389 C>T maps to NM_000137.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr15:80478521 A>T maps to NM_000137.1 K411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:80454613 C>A maps to NM_000137.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:96071536 C>T maps to NM_016044.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr1:207087142 G>T maps to NM_005449.4 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:207085124 G>C maps to NM_005449.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr17:74261642 G>A maps to NM_182565.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:124798881 C>T maps to ENST00000389727 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr17:71228241 G>A maps to NM_001098832.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:55172680 G>T did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr5:14610392 C>T maps to NM_019018.2 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:14690236 C>T maps to NM_138348.4 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr5:14678871 G>T maps to NM_138348.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:1881262 G>A maps to NM_031213.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr8:59058839 C>A maps to NM_147189.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:59058960 A>T maps to NM_147189.2 K58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:58920583 G>A maps to NM_198847.2 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr11:58920508 A>T maps to NM_198847.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:58892263 C>A maps to NM_198947.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:58892346 A>G maps to NM_198947.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:47629445 C>T maps to NM_138371.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:143573428 G>A maps to NM_014719.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr7:143556249 C>T maps to NM_014719.1 W724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr7:143573131 C>T maps to NM_014719.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:143421744 C>T maps to ENST00000441159 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr22:50754501 G>A maps to NM_001001794.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr22:50750579 C>T maps to NM_001001794.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr17:47794917 A>G maps to NM_030802.3 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr2:203622138 G>T maps to NM_173511.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr22:45731234 T>A maps to NM_017911.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr9:96326820 A>G maps to ENST00000333936 *1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:96212823 G>A maps to NM_198841.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:54099691 A>T did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:54107769 C>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:54161492 C>G did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr13:25745388 C>A maps to NM_152704.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:63412921 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:63411078 C>G did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:63412727 C>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:63412738 C>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:63412888 C>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:63411932 T>G did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:63412769 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:63410978 G>A did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:63411390 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:131520088 G>A maps to NM_001105195.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr2:131520796 C>T maps to NM_001105195.1 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:131520907 C>G maps to NM_001105195.1 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:131520538 C>A maps to NM_001105195.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr2:131519749 C>A maps to NM_001105195.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:131520796 C>T maps to NM_001105195.1 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:131520131 C>T maps to NM_001105195.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:17531168 C>T maps to NM_138401.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr19:17534528 G>A maps to NM_138401.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:17531189 C>T maps to NM_138401.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr9:129184186 G>A maps to NM_033446.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:201846387 G>A maps to NM_173822.3 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:134166518 G>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:134186114 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:134185838 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:134156423 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:184853812 C>T maps to NM_052966.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:184859325 G>T maps to NM_052966.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr1:184764869 G>A maps to NM_052966.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:184853878 T>C maps to NM_052966.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr1:184764866 C>T maps to NM_052966.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr19:17651384 C>A maps to ENST00000335393 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:17643148 C>T maps to ENST00000335393 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:17653072 C>T maps to ENST00000335393 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:184062658 A>G maps to NM_144635.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:143053858 C>A maps to NM_001031690.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:92964596 A>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:220047132 C>T maps to NM_024293.4 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr5:16475278 A>G maps to NM_001034850.1 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr6:71185224 A>G maps to NM_001162529.1 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:71236200 G>C maps to NM_001162529.1 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:139144925 C>T maps to NM_015912.3 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:139153477 C>A maps to NM_015912.3 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr8:139263205 C>A maps to NM_015912.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:139190801 G>A maps to NM_015912.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:139144862 C>T maps to NM_015912.3 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr8:139158240 A>T maps to NM_015912.3 P1167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr8:139155319 C>T maps to NM_015912.3 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr8:139149432 G>T maps to NM_015912.3 A1324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:139163693 G>T maps to NM_015912.3 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr8:139164353 G>C maps to NM_015912.3 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:139165195 G>A maps to NM_015912.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr8:139190840 C>A maps to NM_015912.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr8:139255188 G>T maps to NM_015912.3 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr8:139180279 G>A maps to NM_015912.3 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr8:139263258 T>A did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr8:139163750 C>A maps to NM_015912.3 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr2:70528036 C>A maps to ENST00000430566 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr4:89671651 G>A maps to NM_014883.2 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:89668799 G>A maps to NM_014883.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:137284745 G>T maps to NM_016603.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:137346822 C>A maps to NM_016603.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr10:61029735 G>T maps to ENST00000442566 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:61112200 T>A maps to ENST00000442566 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr10:61022301 C>G maps to ENST00000442566 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr4:187093066 G>C did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:53452397 C>G maps to NM_207413.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:18950895 A>G maps to NM_153707.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr15:82575396 C>G maps to NM_001008226.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr13:108518490 G>T maps to NM_001080396.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:68749657 C>G did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:68725501 C>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr14:24610495 G>A maps to NM_016049.3 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:53122664 G>T maps to NM_001042693.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:53122609 C>T maps to NM_001042693.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:6245016 T>A maps to NM_032127.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:6238898 T>A maps to NM_032127.3 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr10:116596001 A>G maps to NM_020940.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr14:74409389 G>A maps to NM_152445.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:75537470 G>A maps to NM_024643.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:140140244 C>T maps to NM_001001710.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr5:74077737 C>T maps to NM_015566.1 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr15:98984299 C>T maps to NM_182562.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr10:15296786 C>A maps to NM_001010924.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:15296870 C>A maps to NM_001010924.1 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:15255180 C>A maps to NM_001010924.1 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr2:187627144 G>C maps to NM_177454.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:187626262 C>A maps to NM_177454.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr2:187627520 G>T maps to NM_177454.3 E818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr10:126523296 A>G maps to NM_032182.3 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr10:102689089 A>T maps to NM_001136123.1 K687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:102716224 C>A maps to NM_001136123.1 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:29259411 T>C maps to NM_199280.2 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr2:29245096 C>A maps to NM_199280.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:135418971 G>A maps to NM_205855.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr7:135418839 G>C maps to NM_205855.3 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:82443574 G>T maps to NM_175885.3 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr1:43613720 C>A maps to NM_001101376.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:35719355 G>A maps to NM_152481.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:35719439 C>A maps to NM_152481.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr10:15885220 C>A maps to NM_024948.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:30868294 G>A maps to NM_032222.2 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:30831178 C>T maps to NM_032222.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr7:30831047 G>T maps to NM_032222.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:30915169 G>T maps to ENST00000509504 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr17:18694244 A>T maps to NM_016078.4 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr4:91389383 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr4:91229476 G>T maps to NM_001145065.1 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:57207712 C>T maps to NM_024946.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr16:57188237 G>T maps to NM_024946.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr3:150377747 A>C maps to NM_152394.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:128974269 G>A maps to NM_001039762.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr10:128936118 C>T maps to NM_001039762.2 W474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr10:128973696 C>T maps to NM_001039762.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr10:128973729 C>G maps to NM_001039762.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:103432833 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:103432969 C>A did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:62148663 G>C maps to NM_178539.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr22:49103556 T>A maps to ENST00000336769 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr22:49042448 C>T maps to ENST00000336769 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr7:195586 C>G maps to NM_020223.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr7:208895 A>C did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr9:99699592 G>A maps to NM_001170741.1 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr9:99699494 G>T maps to NM_001170741.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:10680350 C>T maps to NM_022068.2 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:10696073 C>T maps to NM_022068.2 E2283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:110594510 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:129096368 C>T maps to ENST00000450266 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:194408706 C>A maps to NM_153690.4 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:194407899 G>A maps to NM_153690.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:120867504 G>T maps to NM_207009.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr6:82461467 G>A maps to ENST00000369756 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:79698638 G>C did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:34149720 C>T did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:34148817 C>G did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:34149075 G>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:34150173 G>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:34149281 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:34148159 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:34148341 G>C did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:34148708 C>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:34149268 T>C did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:34149329 C>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:34148450 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:34148668 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:34149882 C>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:34149281 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:34150181 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:34148946 G>C did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:34148515 T>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:34148938 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:34148684 C>A did not map to a codon.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr23:34149039 A>G did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:34961692 G>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:34962362 T>G did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:34961383 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:34962129 G>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:34961595 C>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:34961940 C>G did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:34962425 A>C did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:34962133 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:37029129 C>T did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:37028586 C>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:37026658 G>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:37029126 T>G did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:37028947 C>G did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:37028237 G>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:37028814 C>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:37028599 C>A did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:37029403 A>T did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:37028983 G>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:37027834 G>C did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:37027929 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:37028016 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:37028890 C>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:37026509 G>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:37027656 C>G did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:37028553 C>T did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:37029563 C>A did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr23:37028783 T>A did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:37027906 G>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:37026572 C>T did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr23:37026696 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:37029200 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:37027711 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:37027450 C>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:37028696 C>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr13:37593481 G>T maps to NM_001014286.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr13:37605725 A>T maps to NM_001014286.2 L300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:24382662 G>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:24381381 C>G did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:24382816 A>G did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:24382695 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:24381385 C>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:24330732 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:16740832 C>T maps to NM_030797.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:130874573 G>A maps to NM_016623.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr8:130861551 A>G maps to NM_016623.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr23:153674213 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:153678435 G>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:153678267 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:101520113 C>T maps to NM_145037.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:101540797 G>T maps to NM_145037.2 *560Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr3:101535661 C>T maps to NM_145037.2 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:101540527 C>G maps to NM_145037.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:114453662 C>G maps to NM_001077639.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr11:114441737 T>C maps to NM_001077639.1 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr17:641262 C>G maps to NM_024792.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr17:641209 C>T maps to NM_024792.1 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:200183140 C>G maps to NM_001105517.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:200183002 C>A maps to NM_001105517.1 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:200183330 G>T maps to NM_001105517.1 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:200182883 G>T maps to NM_001105517.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:29850232 C>T maps to ENST00000269209 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:177250055 C>T maps to NM_021165.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:190067165 C>G maps to NM_199051.1 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:190234021 G>A maps to NM_199051.1 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:190067720 G>A maps to NM_199051.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:150971879 G>A maps to NM_001163258.1 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:150971964 C>T maps to NM_001163258.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:150971967 G>A maps to NM_001163258.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:150971904 C>T maps to NM_001163258.1 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:67572953 A>T maps to NM_001193523.1 K127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:67579916 G>A maps to NM_001193523.1 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:24848349 G>C maps to NM_014722.2 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:49236647 G>A maps to NM_080829.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr20:49218869 C>A maps to NM_080829.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr20:49224933 C>T maps to NM_080829.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr20:49214213 C>A maps to NM_080829.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr20:49209623 C>T maps to NM_080829.2 Q770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:139616740 C>T maps to NM_152421.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:119394784 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:119410744 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:212798764 C>T maps to NM_153606.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:156590132 C>G maps to NM_130899.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr5:156592795 C>A maps to NM_130899.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:67664901 T>C maps to NM_173526.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:128369983 C>T maps to NM_032599.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr9:134136487 G>C maps to NM_033387.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:166039930 G>A maps to NM_001017961.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:94727107 C>T maps to NM_152548.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr15:41029864 G>A maps to NM_018145.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:124206349 C>T maps to NM_032899.4 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr6:54805160 G>T maps to NM_001010872.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr6:54735283 T>C maps to NM_001010872.1 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:54805607 C>A maps to NM_001010872.1 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:33880011 C>G maps to NM_178468.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr20:33876707 G>C maps to NM_178468.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr20:33874541 C>A maps to NM_178468.4 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:33875021 C>T maps to NM_178468.4 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:37580565 T>C maps to NM_030919.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:37555034 C>A maps to NM_030919.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr22:40417596 C>T maps to NM_138435.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr22:40415246 C>A maps to NM_138435.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr8:144808384 T>C maps to NM_198488.3 P1082P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:127569403 C>G maps to NM_174911.4 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr16:5143508 G>T maps to NM_201400.2 C72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr12:8376646 C>T maps to NM_018088.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:8374447 G>C maps to NM_018088.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:8376802 G>T maps to NM_018088.3 C44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:8376047 C>G maps to NM_018088.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:94717141 C>T maps to ENST00000452913 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:85132793 G>C maps to ENST00000393246 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:33810283 C>T maps to ENST00000395190 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:38765758 G>T maps to NM_173611.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:8768139 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:8998329 G>A did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr16:89838109 C>A maps to NM_000135.2 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr16:89858947 A>G maps to NM_000135.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:14883177 A>C did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:14861741 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:14861979 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:14861876 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:35423604 G>T maps to NM_021922.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr2:58425767 C>A maps to NM_001114636.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:58392928 G>T maps to NM_001114636.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr14:45658088 G>T maps to NM_020937.2 E1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr14:45623898 G>T did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr14:45645811 T>C maps to NM_020937.2 H1285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr10:127677167 G>C maps to ENST00000368692 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:127685988 G>A maps to ENST00000368692 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:163076374 A>C maps to NM_004460.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:163072484 C>A maps to NM_004460.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:163059574 A>G maps to NM_004460.2 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:13729620 T>C maps to NM_032228.5 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:29423492 G>A maps to NM_018099.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:29469879 G>A maps to NM_018099.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr12:29423456 G>T maps to NM_018099.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr13:99099053 C>T maps to NM_005766.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:99042239 G>C maps to NM_005766.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:242407664 G>A maps to NM_014808.2 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:242407694 G>T maps to NM_014808.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr2:242371149 G>A maps to NM_014808.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr2:242373647 G>T maps to NM_014808.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:242432342 G>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:223436658 G>A maps to NM_005687.3 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr10:90770325 A>T maps to NM_000043.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:172628634 C>A maps to NM_000639.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:80045899 G>A maps to NM_004104.4 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:80053235 C>T maps to NM_004104.4 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:80040802 G>A maps to NM_004104.4 S1918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:80037472 C>T maps to NM_004104.4 A2386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr17:80039489 C>A maps to NM_004104.4 V2131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:187584746 G>A maps to ENST00000260147 R1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr4:187630180 C>A maps to ENST00000260147 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr4:187535498 C>G did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:187539650 C>A maps to ENST00000260147 E2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr4:187541366 C>A maps to ENST00000260147 E2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:187517902 G>T maps to ENST00000260147 S4267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:187584458 T>A maps to ENST00000260147 K1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr4:187541111 C>A maps to ENST00000260147 E2213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr4:187628542 G>A maps to ENST00000260147 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr4:187540390 G>C maps to ENST00000260147 S2453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr4:187541798 G>A maps to ENST00000260147 Q1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr4:187509793 T>C maps to ENST00000260147 E4576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr4:187539059 C>A maps to ENST00000260147 E2897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr4:187554966 G>A maps to ENST00000260147 Y1398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr4:187628793 G>A maps to ENST00000260147 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr4:187539651 C>T maps to ENST00000260147 P2699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr4:187540390 G>C maps to ENST00000260147 S2453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr4:187540704 G>A maps to ENST00000260147 L2348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:187541652 T>C maps to ENST00000260147 S2032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:187541592 C>A maps to ENST00000260147 V2052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:150945549 G>A maps to NM_001447.2 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:150947367 G>A maps to NM_001447.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr5:150948428 G>A maps to NM_001447.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:150945453 G>A maps to NM_001447.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:150946709 G>A maps to NM_001447.2 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:150925110 G>A maps to NM_001447.2 I1859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:150925890 G>A maps to NM_001447.2 S1599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:150929056 G>A maps to NM_001447.2 Q1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr5:150945542 C>A maps to NM_001447.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:92533402 C>T maps to ENST00000298047 P2408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:92534584 C>T maps to ENST00000298047 I2802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:92590383 A>T maps to ENST00000298047 G3790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:92087083 G>A maps to ENST00000298047 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:92088253 C>A maps to ENST00000298047 I992I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:92534452 A>T maps to ENST00000298047 I2758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:92564923 G>T maps to ENST00000298047 R3206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:92533300 G>A maps to ENST00000298047 L2374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:92568144 C>A maps to ENST00000298047 V3327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:92495062 C>A maps to ENST00000298047 T1237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:92534953 G>T maps to ENST00000298047 A2925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:92616491 C>T maps to ENST00000298047 P4290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr11:92495110 G>A maps to ENST00000298047 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:92087129 G>T maps to ENST00000298047 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr11:92616284 C>G maps to ENST00000298047 V4221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:92600238 G>T maps to ENST00000298047 P3997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr11:92533600 G>A maps to ENST00000298047 G2474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr11:92624032 G>T maps to ENST00000298047 P4508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:126402737 C>T maps to NM_024582.4 Q4221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr4:126411434 G>T maps to NM_024582.4 G4486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:126371353 A>G maps to NM_024582.4 A3061A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:126389769 A>G maps to NM_024582.4 K4001K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:126241564 C>T maps to NM_024582.4 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr4:126336606 T>C maps to NM_024582.4 I2163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr4:126238159 G>T maps to NM_024582.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr4:126241387 C>T maps to NM_024582.4 D1274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:126242173 T>A maps to NM_024582.4 A1536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr4:126328187 C>T maps to NM_024582.4 Q1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:126240598 G>T maps to NM_024582.4 V1011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:126369934 C>T maps to NM_024582.4 T2588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:150891114 C>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:150891156 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr19:40330879 G>T maps to NM_001436.3 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr3:13671365 G>A maps to NM_001165035.1 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:112945055 C>A maps to NM_153214.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:48903021 G>A maps to NM_000138.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr15:48796074 C>T maps to NM_000138.4 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:48788312 A>G maps to NM_000138.4 D801D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr15:48782116 C>A maps to NM_000138.4 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr15:48789499 T>C maps to NM_000138.4 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr15:48717599 G>T maps to NM_000138.4 G2473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr15:48826373 C>A maps to NM_000138.4 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:127648326 G>A maps to NM_001999.3 S1626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr5:127729061 C>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:127670447 C>G maps to NM_001999.3 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr5:127674727 A>T maps to NM_001999.3 P1123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:127671678 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr5:127636599 G>T maps to NM_001999.3 G2025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr5:127648419 G>A maps to NM_001999.3 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:127744402 C>A maps to NM_001999.3 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:127614474 G>C maps to NM_001999.3 S2399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:8151967 G>A maps to NM_032447.3 G2249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:8161783 C>G maps to NM_032447.3 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr19:8203326 C>T maps to NM_032447.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:8136934 G>A maps to NM_032447.3 H2695H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:8130937 C>A maps to NM_032447.3 R2765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr9:97333767 G>C maps to NM_003837.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:102665557 C>T maps to NM_145032.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:102667931 T>C maps to NM_145032.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:1702722 G>T maps to NM_152441.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:745746 C>A maps to NM_153350.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr16:746774 C>A maps to NM_153350.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr7:5540480 G>A maps to ENST00000312577 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr17:37420577 G>T maps to NM_032875.2 C351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:135276948 C>T maps to NM_012159.4 H298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr13:77589612 G>A maps to NM_012158.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr13:77581288 G>C maps to NM_012158.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr9:37537355 C>T maps to NM_012166.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:37541207 T>A maps to NM_012166.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:71796838 A>G maps to NM_001142958.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr8:28321167 A>G maps to NM_172366.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr10:5948138 C>T maps to NM_032807.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:11708777 G>A maps to NM_012168.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:117595835 T>A maps to NM_033624.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr12:117610394 T>A maps to NM_033624.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr19:39516089 C>T maps to NM_178820.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr16:87393973 T>G did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:124553143 G>A maps to NM_058229.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:124553155 G>A maps to NM_058229.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:147821649 G>T maps to NM_205836.1 V1169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr5:41927171 G>T maps to NM_012176.2 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:121340660 C>T maps to NM_016298.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr3:121340299 G>T maps to NM_016298.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:73487571 C>T maps to ENST00000295133 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:16577479 G>A maps to NM_018994.1 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:16577800 C>G maps to NM_018994.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:101149791 C>A did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:11721283 C>T maps to ENST00000376768 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:46215940 G>T maps to NM_001080469.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr19:46215709 G>T maps to NM_001080469.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr17:18668085 C>T maps to ENST00000395665 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr5:171305016 C>A maps to NM_012300.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr3:48423470 C>A maps to NM_207102.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr4:153244193 C>A maps to NM_033632.2 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr4:153244197 C>G maps to NM_033632.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr4:153247366 G>A maps to NM_033632.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:153244123 G>C maps to NM_033632.2 S678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:153249409 G>T maps to NM_033632.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:153247366 G>T maps to NM_033632.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr12:117402576 C>T maps to NM_153348.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:12800823 G>A maps to ENST00000380339 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr1:159277607 A>G maps to ENST00000368115 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:159273817 C>T maps to ENST00000368115 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:159275871 G>A maps to ENST00000368115 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:159275931 C>T maps to ENST00000368115 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:159277626 C>T maps to ENST00000368115 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:159275862 T>C maps to ENST00000368115 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:7762179 C>A maps to NM_002002.4 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:40362802 G>A maps to NM_003890.2 F5089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:40433635 C>T maps to NM_003890.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr19:40367870 T>G maps to NM_003890.2 P4363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:40433440 C>A maps to NM_003890.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr19:40420080 C>T maps to NM_003890.2 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:40357379 C>A maps to NM_003890.2 V5311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:40433533 C>T maps to NM_003890.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:40368471 G>A maps to NM_003890.2 T4292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:149763060 G>A maps to NM_000566.3 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:149761655 C>T maps to NM_000566.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:161560952 C>G maps to NM_201563.4 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:161559370 G>T maps to NM_201563.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:161518411 T>A maps to NM_000569.6 K76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:161518241 G>T maps to NM_000569.6 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:161599598 G>T maps to ENST00000367964 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:50017654 C>T maps to NM_004107.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr5:141029087 G>A maps to ENST00000354789 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:72712088 G>A maps to ENST00000409314 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr9:137802991 G>T maps to NM_002003.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr9:137774435 G>T maps to NM_004108.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:157772323 C>A maps to NM_052938.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:157771326 G>T maps to NM_052938.4 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:157772250 C>A maps to NM_052938.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:157740376 C>T maps to NM_030764.3 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr1:157738318 C>G maps to NM_030764.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:157738267 A>T maps to NM_030764.3 Y273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:157718391 C>T maps to NM_030764.3 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr1:157740400 C>G maps to NM_030764.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:157668204 G>C maps to NM_052939.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:157667698 G>T maps to NM_052939.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:157659609 G>A maps to NM_052939.3 Y596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:157665334 G>A maps to NM_052939.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:157660174 G>A maps to NM_052939.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:157666082 C>A maps to NM_052939.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr1:157555964 A>C maps to NM_031282.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:157548309 C>T maps to NM_031282.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:157559033 G>A maps to NM_031282.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:157490978 C>T maps to NM_031281.2 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:157509154 C>A did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:157514127 C>A maps to NM_031281.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:157485496 G>A maps to NM_031281.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:157514825 A>G maps to NM_031281.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:157491041 C>A maps to NM_031281.2 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:159778966 G>A maps to NM_001004310.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:159785345 G>A maps to NM_001004310.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:159779426 C>T maps to NM_001004310.2 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:161697325 G>T maps to NM_001002901.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr18:55221490 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr18:55247366 G>A maps to NM_001012515.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:4793665 G>C maps to NM_018708.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr15:68582854 C>T maps to NM_015322.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:108207796 A>T maps to NM_005246.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:125076648 C>T maps to NM_001039112.2 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:125107242 G>A maps to NM_001039112.2 R1553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr8:125072482 C>A maps to NM_001039112.2 Y979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:125035682 G>C did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr8:124978245 G>T did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr7:19184778 C>A maps to NM_152898.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:19184886 G>A maps to NM_152898.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:53417130 G>T maps to NM_001134999.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:63990579 C>T maps to NM_178443.2 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:63987219 C>A maps to NM_178443.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:63978759 A>G maps to NM_178443.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr15:91428388 C>G maps to NM_002005.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr15:91428340 C>A maps to NM_002005.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:186362639 T>C maps to NM_014375.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:186358323 C>A maps to NM_014375.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:125359547 G>T maps to NM_005103.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:121944014 G>T maps to NM_001024613.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr7:121943743 G>A maps to NM_001024613.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr7:121942910 T>A maps to NM_001024613.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:121944014 G>A maps to NM_001024613.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:62358018 C>A maps to NM_018008.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr3:62357264 G>A maps to NM_018008.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:35941491 G>A maps to NM_005306.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr19:35940861 C>A maps to NM_005306.2 C82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:35849878 C>A maps to NM_005304.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:35849929 C>T maps to NM_005304.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:35849878 C>G maps to NM_005304.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:155508747 C>T maps to NM_000508.3 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:155507005 A>T maps to NM_000508.3 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr4:155507371 C>T maps to NM_000508.3 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:54481901 C>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:54482794 C>T did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:54472817 G>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:54476174 G>T did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr6:36982741 C>G maps to NM_173558.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr3:14862233 C>T maps to NM_152536.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:44310603 G>A maps to NM_004465.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:44388622 G>T maps to NM_004465.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr3:192125874 G>T maps to NM_021032.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:192078313 T>C maps to NM_021032.4 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:192125892 C>A maps to NM_021032.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:137715013 C>G did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:137791013 G>C did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:123797542 C>A maps to NM_002006.4 Y215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:16850673 G>A maps to NM_019851.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:69631135 G>A maps to NM_005247.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:81207574 C>A maps to NM_004464.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:49716679 G>A maps to NM_002009.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr8:38271764 G>A maps to NM_001174067.1 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr10:123263410 C>G maps to ENST00000351936 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:1018452 G>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr4:155530894 T>A maps to ENST00000407946 K193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr8:17722241 C>T maps to NM_201552.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:241669321 T>C maps to NM_000143.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:241667397 G>T maps to NM_000143.3 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr4:153897749 G>T maps to NM_033393.2 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:60522644 G>C maps to NM_002012.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:135290626 G>C did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr6:97053850 T>C maps to NM_020482.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:97063548 C>T maps to NM_020482.4 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr6:97058602 C>T maps to NM_020482.4 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr18:34359420 C>A maps to NM_025135.2 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:27016313 C>A maps to NM_203371.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr11:27016498 C>T maps to NM_203371.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr11:27016327 C>A maps to NM_203371.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:15364279 C>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:15365295 C>G did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:15381378 C>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:71012600 A>G maps to NM_001004311.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:164466955 C>T maps to NM_018086.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:164467849 T>A maps to NM_018086.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr2:164466433 T>A maps to NM_018086.2 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr2:164467189 G>A maps to NM_018086.2 S384S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-85-6561-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:76023519 G>A maps to NM_015687.2 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr6:76022256 C>T maps to NM_015687.2 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:76022792 C>A maps to NM_015687.2 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:99552093 A>T maps to NM_182909.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:54319141 C>A maps to NM_030917.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:115956356 G>T maps to ENST00000446284 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr9:115940911 G>C maps to ENST00000446284 S720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr9:115964867 T>C maps to ENST00000446284 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:2906970 A>G maps to NM_002014.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr7:72744315 G>A maps to NM_003602.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:72742585 C>T maps to NM_003602.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:72756881 A>T maps to NM_003602.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:72754818 C>T maps to NM_003602.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:27293585 A>G maps to NM_032030.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:108366509 G>T maps to NM_006731.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr9:108366569 C>T maps to NM_006731.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr17:17131271 C>A maps to NM_144997.5 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:17122398 G>A maps to NM_144997.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:17129540 G>C maps to NM_144997.5 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr1:152280464 G>T maps to NM_002016.1 S2299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:152283956 C>T maps to NM_002016.1 R1135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:152285256 G>C maps to NM_002016.1 S702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:152277173 A>T maps to NM_002016.1 S3396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:152286977 C>T maps to NM_002016.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:152284055 G>A maps to NM_002016.1 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:152283854 C>T maps to NM_002016.1 P1169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:152281207 C>A maps to NM_002016.1 E2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:152279084 A>G maps to NM_002016.1 T2759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr1:152283512 G>A maps to NM_002016.1 S1283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:152276144 G>A maps to NM_002016.1 H3739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:152282837 T>G maps to NM_002016.1 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:152279631 G>C maps to NM_002016.1 S2577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:152277863 A>G maps to NM_002016.1 R3166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:152276038 C>A maps to NM_002016.1 E3775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:152328899 G>T maps to NM_001014342.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr1:152323610 C>T maps to NM_001014342.2 G2217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:152329580 A>T maps to NM_001014342.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:152329649 C>T maps to NM_001014342.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr1:152327319 G>T maps to NM_001014342.2 S981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:152325500 C>T maps to NM_001014342.2 G1587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:152328464 G>T maps to NM_001014342.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:152323766 G>A maps to NM_001014342.2 S2165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr11:128628019 C>A maps to NM_002017.3 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:128638129 C>T maps to NM_002017.3 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:18149710 G>A maps to NM_002018.2 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:21552085 G>A maps to NM_018071.3 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:21547126 G>T maps to NM_018071.3 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:142506591 G>A maps to NM_207414.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr8:142477648 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:142458035 G>T maps to NM_207414.2 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:142476591 G>A maps to NM_207414.2 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:142500316 G>A maps to NM_207414.2 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:84606845 A>G maps to NM_001001670.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:84610037 T>C maps to NM_001001670.2 F1551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr9:84607400 C>T maps to NM_001001670.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr9:84606391 C>A maps to NM_001001670.2 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr9:84608636 T>C maps to NM_001001670.2 D1084D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr9:84606080 G>A maps to NM_001001670.2 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr9:84608129 G>T maps to NM_001001670.2 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:153577260 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:153587669 G>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:153587657 C>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:153595789 C>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:153580936 G>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:153589881 G>C did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:153596278 T>C did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:153582285 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:153581666 C>T did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr23:153594530 T>C did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:153594738 G>T did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:153589927 A>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:153577266 A>T did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:153581948 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:153582817 G>A did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr23:153592741 T>G did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:153585880 G>A did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:153578189 C>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:58090917 C>A maps to NM_001164317.1 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:58156458 T>C maps to NM_001164317.1 P2624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:58089693 G>T maps to NM_001164317.1 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:58134385 C>T maps to NM_001164317.1 F1997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:58112436 C>T maps to NM_001164317.1 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:128478325 C>A maps to NM_001458.4 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:128497373 C>T maps to NM_001458.4 F2588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:128493534 T>A maps to NM_001458.4 L2074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr7:128484995 G>T maps to NM_001458.4 R1159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr7:128486410 C>T maps to NM_001458.4 R1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:128494158 C>A maps to NM_001458.4 R2206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:128496853 C>A maps to NM_001458.4 V2480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr7:128492891 C>T maps to NM_001458.4 F2005F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:128485259 G>A maps to NM_001458.4 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:128480701 G>T maps to NM_001458.4 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:30697819 G>C maps to NM_005803.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:30707976 G>C maps to NM_005803.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:86088739 G>T maps to NM_013231.4 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr14:86088140 C>T maps to NM_013231.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:86088820 C>T maps to NM_013231.4 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr13:29008090 G>C maps to NM_002019.4 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr13:29041226 C>T maps to NM_002019.4 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:28588654 C>T maps to NM_004119.2 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr13:28623590 T>C maps to NM_004119.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr13:28624271 T>C maps to NM_004119.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:180047185 C>T maps to NM_182925.4 E843E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:180043932 C>T maps to NM_182925.4 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:180048824 T>C maps to NM_182925.4 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:180056732 G>C maps to NM_182925.4 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr14:76101272 A>G maps to NM_017791.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr16:2983293 A>G maps to ENST00000399667 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr16:2946557 C>T maps to NM_138439.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:240497431 C>A maps to ENST00000406993 L1699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:240370311 C>A maps to ENST00000406993 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:240371820 C>T maps to ENST00000406993 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:240255882 G>A maps to ENST00000406993 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:240256011 G>A maps to ENST00000406993 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:240519116 C>A maps to ENST00000406993 A1732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:240497230 C>T maps to ENST00000406993 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:240371435 T>C maps to ENST00000406993 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr17:43319801 C>T maps to NM_005892.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:171250058 G>A maps to NM_002021.1 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:171251428 T>A maps to NM_002021.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:171251338 C>A maps to NM_002021.1 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:171086460 C>A maps to NM_006894.5 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:171073020 T>C maps to NM_006894.5 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:171303693 G>C maps to NM_002022.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:171292328 A>T maps to NM_002022.1 K107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr1:146684905 G>T maps to NM_001461.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:147024823 A>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:147009841 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:147018993 C>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:147024735 G>C did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:147030326 T>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:147011671 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:147106425 T>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:147063147 A>G did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr2:216269277 C>T maps to NM_212482.1 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:216293050 G>A maps to NM_212482.1 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:216300471 C>G maps to NM_212482.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:216296608 A>C maps to NM_212482.1 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:216285489 C>G maps to NM_212482.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr2:216288135 T>A maps to NM_212482.1 K444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr9:132689608 C>T maps to NM_015033.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:159653083 T>C maps to NM_032532.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:159653964 G>T maps to NM_032532.2 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:159677648 A>G maps to NM_032532.2 L1720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr6:159653352 C>T maps to NM_032532.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr13:49772212 A>C maps to NM_001079673.1 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr13:49710672 A>G maps to NM_001079673.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr3:172096200 C>G maps to NM_022763.3 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr3:172052808 G>T maps to NM_022763.3 G573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:171851308 G>T maps to NM_022763.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr1:109265068 C>T maps to NM_001144937.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:33456481 C>T maps to NM_017559.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr5:131008212 C>A maps to NM_133372.2 G642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr5:131008510 A>G maps to NM_133372.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:159790430 C>T maps to ENST00000379346 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr4:159791563 C>G maps to ENST00000379346 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr8:42932393 G>T maps to NM_002027.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:49175954 T>C maps to NM_004476.1 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:49175784 G>T maps to NM_004476.1 S628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:49207290 A>T maps to NM_004476.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr11:49179592 C>T maps to NM_004476.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:89424613 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:89429875 A>T maps to NM_153696.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr11:89431763 C>A maps to NM_153696.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr11:71850517 G>A maps to ENST00000442948 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:45975849 G>T maps to NM_006732.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:65664330 G>A maps to NM_005438.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr15:60298007 C>A maps to NM_012182.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:60298079 C>A maps to NM_012182.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr9:79634611 G>T maps to NM_001013735.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr9:79635628 C>T maps to NM_001013735.1 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:1611180 C>T maps to NM_001453.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:86602311 C>T maps to NM_005251.2 H457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:47904254 T>C maps to NM_004474.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr9:117744 G>C maps to NM_207305.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:114257216 C>G maps to NM_012184.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr16:86544552 G>C maps to NM_001451.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:1390511 C>T maps to NM_001452.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:1390814 G>T maps to NM_001452.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:29237354 G>C maps to NM_005249.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:29237480 G>A maps to NM_005249.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:169535119 G>A maps to NM_012188.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr5:169535449 G>T maps to NM_012188.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:169533462 C>T maps to NM_012188.4 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr5:169533491 C>T maps to NM_012188.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr10:129537211 G>T maps to NM_207426.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:8203145 C>T maps to NM_018416.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:42654555 A>C maps to NM_001198850.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:26861380 G>A maps to NM_003593.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr17:26851654 C>T maps to NM_003593.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:48573598 T>C maps to NM_002158.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr2:48602578 A>G maps to NM_002158.3 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:89878559 G>T maps to NM_001085471.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr14:89656794 T>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:109724542 C>T maps to NM_213596.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:109719362 G>T maps to NM_213596.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:108985286 C>A maps to NM_001455.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:70316675 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:70321013 C>G did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:70321031 C>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:70320606 C>G did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:71015078 C>T maps to NM_032682.4 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr3:71090509 G>A maps to NM_032682.4 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr7:114298203 A>T maps to NM_148898.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:114271686 C>T maps to NM_148898.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:49107901 G>A did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:118851316 C>T maps to NM_181721.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr23:55650441 G>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:55650590 C>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:55650239 G>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:126146369 C>A maps to NM_017547.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:74670222 T>A maps to NM_003838.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:74670657 A>G maps to NM_003838.3 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:74665363 T>C maps to NM_001112808.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:74670300 T>G maps to NM_003838.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:52249566 C>T maps to NM_002029.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:52272531 C>A maps to NM_001005738.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:52327117 C>T maps to NM_002030.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr10:95441273 T>C maps to NM_145246.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr4:79308542 G>C maps to NM_025074.6 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr4:79322021 A>G maps to NM_025074.6 T1370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr4:79418101 C>A maps to NM_025074.6 S3034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr10:99093813 G>A maps to NM_012083.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr9:14776176 C>A maps to ENST00000380880 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr9:14788992 G>A maps to ENST00000380880 F1370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr9:14824963 C>A maps to ENST00000380880 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr9:14775879 A>G maps to ENST00000380880 T1591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr9:14759787 C>A maps to ENST00000380880 S1775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr9:14857663 C>A maps to ENST00000380880 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr9:14846057 G>T maps to ENST00000380880 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:14737562 C>T maps to ENST00000380880 W2127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr9:14801697 G>A maps to ENST00000380880 Q1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr13:39452268 A>T did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr13:39271907 T>C maps to NM_207361.4 F1749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:190883075 G>T maps to NM_004477.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:135440162 G>T maps to ENST00000443774 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:116289833 G>A maps to NM_002031.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr6:116289817 G>T maps to NM_002031.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr6:116289810 C>T maps to NM_002031.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:116288786 A>T maps to NM_002031.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:69435101 C>A maps to NM_015123.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr15:44211709 G>A maps to NM_032892.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr14:52182110 C>A maps to ENST00000344768 C306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr14:52192506 G>C maps to ENST00000344768 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:52164868 C>T maps to ENST00000344768 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:131219750 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:131219973 C>G did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:131218579 T>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:131212471 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:65161797 C>G maps to NM_031904.3 Y161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr9:37740468 C>T maps to NM_014907.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr9:37740402 C>G maps to NM_014907.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr9:37746210 G>A maps to NM_014907.2 S1394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr10:49448457 C>T maps to NM_001018071.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:12736380 C>G did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr23:12734275 A>G did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:12735104 G>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:100185122 C>A maps to NM_001013660.2 G363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:100203640 C>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:69968728 C>T maps to NM_006654.3 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr12:69968636 G>T maps to NM_006654.3 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:32841363 C>T maps to NM_023037.2 I2668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr13:32711021 G>T maps to NM_023037.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr13:32709038 A>T did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr13:32705839 G>T maps to NM_023037.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr13:32813924 G>A maps to NM_023037.2 T2198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:48572901 G>A maps to NM_015030.1 R980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:48514563 C>T maps to NM_015030.1 Q2693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:48584728 C>A maps to NM_015030.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr4:48512144 G>C maps to NM_015030.1 L2775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr2:183730875 G>A maps to NM_001463.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:44973931 T>A maps to NM_032135.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:44976160 T>C maps to NM_032135.3 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr14:44974482 C>A maps to NM_032135.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:127235653 G>A maps to NM_020369.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:127240278 C>T maps to NM_020369.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:127235359 G>A did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr19:4318940 A>T maps to NM_024333.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr19:4311904 G>A maps to NM_024333.2 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:49210250 G>T maps to NM_000145.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:49191002 C>T maps to NM_000145.3 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:49195947 G>T maps to NM_000145.3 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:49189949 G>A maps to NM_000145.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:49190183 G>T maps to NM_000145.3 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr15:40030345 C>A maps to NM_152597.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:52780902 G>T maps to NM_013409.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr3:120122197 T>A maps to NM_007085.4 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:120121720 C>A maps to NM_007085.4 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:120130803 C>A maps to NM_007085.4 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr5:132939578 C>A maps to NM_015082.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr4:162307057 C>G maps to NM_020116.3 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr4:162376271 G>T maps to NM_020116.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr4:162402261 A>T maps to NM_020116.3 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:162402217 A>T maps to NM_020116.3 L521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr11:61732987 C>G did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:31089711 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:31089770 G>T did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:31089534 C>G did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr23:31089810 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:31089887 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:49469079 C>T maps to NM_000146.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:49468814 C>G maps to NM_000146.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:121188233 C>T maps to NM_177478.1 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr16:53844089 C>T maps to NM_001080432.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:53913763 A>G maps to NM_001080432.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:48340062 C>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr7:2275029 C>A maps to NM_013393.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr17:61902893 A>G did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr17:61897534 T>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:78414916 C>A maps to ENST00000436586 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr9:133507352 G>T maps to NM_003934.1 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr9:133488373 G>T maps to NM_003934.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:70501322 A>T maps to NM_145059.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr16:70505155 C>A maps to NM_145059.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr16:70504959 G>A maps to NM_145059.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:44383469 C>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:154261827 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:154280052 G>C did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:154261814 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:91424897 C>T maps to NM_002569.2 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr15:91425047 A>T maps to NM_002569.2 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:33310820 A>G maps to ENST00000380081 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr19:5844193 C>A maps to NM_001097641.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:5867625 G>T maps to NM_002034.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr9:139925443 G>T maps to NM_004479.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:66208890 C>T maps to NM_178155.1 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr14:66028289 A>G maps to NM_178155.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr14:66136157 A>T maps to NM_178155.1 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:66096257 T>A maps to NM_178155.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr6:96651799 C>T maps to NM_006581.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:180671548 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:180671611 T>A maps to NM_005087.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:180671623 C>A maps to NM_005087.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr17:7504843 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:7498075 C>G did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr10:43869927 C>A maps to NM_173160.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr19:35649253 C>G maps to NM_001164605.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr5:39135116 C>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr7:90895352 C>T maps to NM_003505.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr12:130648773 G>A maps to NM_007197.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr17:42635358 C>A maps to NM_001466.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr17:42636018 C>T maps to NM_001466.3 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:28385266 G>A maps to NM_017412.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:104330834 A>T maps to NM_003506.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:104340585 G>T maps to NM_003506.3 G495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:202900497 C>A maps to NM_003507.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:202900095 G>T maps to NM_003507.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:35930015 G>A maps to NM_031866.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:76570868 C>A maps to NM_203505.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:41063046 G>T maps to NM_000151.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr17:41052950 C>T maps to NM_000151.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:153774348 T>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr17:78085890 C>T maps to NM_001079804.1 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:144387362 C>A maps to NM_207123.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr4:144390335 G>C maps to NM_207123.2 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:77937951 G>T maps to NM_080491.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:153940623 G>T did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr23:153927771 G>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:153940969 G>A did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr22:17472931 A>G maps to NM_001037814.1 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr22:17443715 C>T maps to NM_001037814.1 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:29574953 G>A maps to NM_001470.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:29574166 C>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:29574953 G>A maps to NM_001470.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:29574775 C>A maps to NM_001470.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr9:101125062 C>G maps to NM_005458.7 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr9:101216304 G>T maps to NM_005458.7 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr21:27141329 G>T maps to NM_002040.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:161300179 A>T maps to NM_001127648.1 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr5:161281236 C>T maps to NM_001127648.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:161281214 C>T maps to NM_001127648.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:46307591 G>T maps to ENST00000507069 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:46305528 G>T maps to ENST00000507069 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:46388099 C>A maps to ENST00000507069 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:151336920 C>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:151366221 T>G did not map to a codon.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr23:151336819 G>A did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:151358287 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:151424345 A>T did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr4:46967067 G>T maps to NM_000809.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr4:46930487 A>G maps to NM_000809.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:27193256 C>A maps to NM_000810.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr15:27126085 C>G maps to NM_000810.3 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr15:27185219 T>G maps to NM_000810.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:161128572 G>T maps to NM_000811.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr4:47428022 C>T maps to NM_000812.3 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:47408750 C>A maps to NM_000812.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr15:26812800 A>T maps to NM_021912.4 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr15:26812773 C>A maps to NM_021912.4 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr15:26812773 C>A maps to NM_021912.4 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr15:26793203 G>T maps to NM_021912.4 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr15:26793166 C>A maps to NM_021912.4 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr15:26806097 G>C maps to NM_021912.4 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:26825603 C>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr15:26866630 G>C maps to NM_021912.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr15:26828551 C>G maps to NM_021912.4 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:1957003 G>A maps to NM_000815.4 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:151130931 G>C did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:151124014 G>A did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr23:151138713 G>C did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr4:46060534 G>T maps to NM_173536.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr4:46053441 G>T maps to NM_173536.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr4:46125864 C>T maps to NM_173536.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr4:46060550 A>G maps to NM_173536.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr4:46043217 A>T maps to NM_173536.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:161495048 C>A maps to NM_198903.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:161495094 G>T maps to NM_198903.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:161524750 C>A maps to NM_198903.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:161576270 C>T maps to NM_198903.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:161580226 C>T maps to NM_198903.2 C467C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:27772742 A>T maps to NM_033223.4 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:27572056 G>T maps to NM_033223.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr15:27725805 C>T maps to NM_033223.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:151821067 T>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:151820228 T>C did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:151818972 C>A did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:151821420 G>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:151815468 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:151821601 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:151821677 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:151817746 G>T did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:151821076 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:151818343 T>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr6:89890083 G>T maps to NM_002042.3 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:97705817 C>T maps to NM_001105580.1 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:97711839 G>A maps to NM_001105580.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:97731303 C>T maps to NM_001105580.1 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:171709292 C>A maps to NM_000817.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:26569997 T>A maps to NM_001134366.1 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr10:26581458 C>T maps to NM_001134366.1 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr10:26534905 G>A maps to NM_001134366.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:26518594 C>A maps to NM_001134366.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr10:26559633 C>G maps to NM_001134366.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr10:26589811 C>A maps to NM_001134366.1 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:49161384 A>T did not map to a codon.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr4:905527 C>G maps to NM_005255.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:853486 G>A maps to NM_005255.2 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr4:853457 G>A maps to NM_005255.2 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr4:887730 G>A maps to NM_005255.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr4:843831 C>A maps to NM_005255.2 E1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr22:30951749 C>T maps to NM_004861.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr22:30951443 G>A maps to NM_004861.1 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr22:30951743 G>A maps to NM_004861.1 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:242738524 C>A maps to NM_022134.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr7:99757892 G>A maps to NM_024637.4 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr14:88417032 T>C maps to NM_000153.2 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:88452845 A>G maps to NM_000153.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr15:49584699 C>G maps to NM_002044.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:38956734 G>T maps to NM_138801.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:88893132 G>A maps to NM_000512.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr16:88902185 C>A maps to NM_000512.4 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:88909126 A>G maps to NM_000512.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr18:33271055 G>A maps to NM_020474.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr18:33234649 G>A maps to NM_020474.3 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr18:33283582 C>T maps to NM_020474.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr18:33272175 G>A maps to NM_020474.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:155102468 G>A maps to NM_052917.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:155265536 C>T maps to NM_052917.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr2:155099238 C>T maps to NM_052917.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr2:155098614 G>A maps to NM_052917.2 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:154801050 C>A maps to NM_052917.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr2:31165142 G>A maps to NM_024572.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:230401026 C>T maps to NM_004481.3 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:158152277 A>G maps to NM_014568.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:158142594 G>T maps to NM_014568.1 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr4:174090000 T>A maps to NM_017423.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr12:132688079 G>A maps to NM_001122636.1 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr14:69813861 C>A maps to NM_020692.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:69787471 G>T maps to NM_020692.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr3:16242201 G>T maps to NM_054110.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:16254179 G>A maps to NM_054110.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:11292797 C>A maps to NM_198516.2 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr7:151704911 G>C maps to NM_145292.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr4:173232903 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:173269754 C>A maps to NM_001034845.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr18:74962935 C>A maps to NM_001480.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr18:74980854 G>A maps to NM_001480.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr22:38219751 G>A maps to NM_003614.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr9:34647933 G>T maps to NM_000155.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr11:62397402 C>T maps to NM_198335.2 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:115395194 G>A maps to NM_001130064.1 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr19:36035844 C>A maps to NM_014364.4 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:36034321 C>A maps to NM_014364.4 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:128099687 C>T maps to NM_015635.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:128117938 C>T maps to NM_015635.2 T1285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr9:128064642 G>T maps to NM_015635.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr9:130098405 G>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr21:34892832 G>A maps to NM_001136006.1 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr22:29706907 G>C maps to NM_152236.1 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr22:29706514 G>C maps to NM_152236.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:101018439 C>T maps to NM_174942.1 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr12:101005804 A>T maps to NM_174942.1 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr12:101005797 G>A maps to NM_174942.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr13:114541066 G>C maps to ENST00000357389 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:9830002 G>A maps to NM_201433.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:9828856 C>T maps to NM_201433.1 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:90103746 G>A maps to NM_001481.2 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr16:90102916 G>T maps to NM_001481.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:48650416 C>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:48652346 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:48652235 C>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr23:48652459 C>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:128204696 G>A maps to NM_032638.4 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:128199972 C>T maps to NM_032638.4 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:8115916 G>T maps to NM_001002295.1 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:8097817 C>A maps to NM_001002295.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:11607693 G>A maps to NM_002052.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:11607645 C>G maps to NM_002052.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr8:11607663 C>A maps to NM_002052.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr18:19780784 G>C maps to NM_005257.3 *596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:19613321 G>T maps to ENST00000404158 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:19612824 C>A maps to ENST00000404158 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr7:99831236 T>C maps to NM_178831.6 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:155208007 G>A maps to NM_001005742.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr4:22748916 A>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr4:22749245 G>A maps to NM_020973.3 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:22749309 G>T maps to NM_020973.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr10:104129062 C>A maps to NM_004193.2 I1022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr10:104140417 A>G maps to NM_004193.2 E1715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:89523673 C>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:89579959 C>T maps to NM_004120.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:89652767 C>T maps to NM_052941.4 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:89652146 C>A maps to NM_052941.4 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:89729532 T>C maps to NM_052942.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:89615178 T>A maps to NM_207398.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:163216740 T>C maps to NM_012198.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr22:38212583 C>G maps to NM_001171690.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:127222463 T>C maps to NM_024523.5 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr7:127222186 G>A maps to NM_024523.5 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:109100634 G>T maps to NM_181453.3 E1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr2:109087167 T>C maps to NM_181453.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:109086492 T>C maps to NM_181453.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:13010342 G>T maps to NM_000159.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:13002939 G>A maps to NM_000159.2 R94R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-66-2755-01A-01D-1522-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-39-5028-01A-01D-1441-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr3:111844070 A>T did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr7:44192987 C>T maps to NM_000162.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:44184788 G>T maps to NM_000162.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:27721619 G>A maps to NM_001486.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:94360224 C>T maps to NM_002061.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr6:52993119 G>A maps to NM_003643.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr6:10876186 G>A maps to NM_004752.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:10874707 G>A maps to NM_004752.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:120582787 C>T maps to NM_006836.1 P1698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr12:120587434 C>T maps to NM_006836.1 E1507E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr12:120606104 C>G did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:59910814 A>G maps to NM_004751.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr15:59910529 C>T maps to NM_004751.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:74810477 G>C maps to ENST00000238018 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr9:74842915 C>T maps to ENST00000238018 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr9:74838033 A>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr9:74860169 G>T maps to ENST00000238018 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:42907843 G>A maps to NM_024034.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr16:19519023 T>C maps to NM_016641.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr10:48429450 C>T maps to NM_004962.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:48429027 G>T maps to NM_004962.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:48413940 A>T maps to NM_016204.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:7842860 C>T maps to NM_020634.1 V236V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-21-5787-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr20:34021837 C>A maps to NM_000557.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:97172860 C>T maps to NM_001001557.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:153668415 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:153668444 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:153669524 G>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:153667171 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr10:5836976 G>A maps to NM_001494.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:69649803 C>G did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:69646854 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:69647201 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr16:30123731 G>A maps to NM_024307.2 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:30123996 C>A maps to NM_024307.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:76969501 C>A maps to ENST00000376217 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:95272460 G>A maps to NM_181702.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:648683 G>A maps to NM_015721.2 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr17:649356 C>T maps to NM_015721.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr5:154316659 G>T maps to NM_015465.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:45593722 G>T maps to NM_024707.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:45593578 C>T maps to NM_024707.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:14027117 T>C did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:14038350 G>C did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:17963068 G>T maps to NM_001130009.1 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:17954484 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:17952507 G>T maps to NM_001130009.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr9:135863680 C>A maps to NM_004188.4 A112A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3411-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:158363991 C>A maps to ENST00000482640 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:158408929 C>T maps to ENST00000264263 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:158409238 G>T maps to ENST00000264263 G766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr2:69569382 T>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr5:179740887 G>A maps to NM_005110.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr20:3640821 C>A maps to NM_145762.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:55214923 A>C maps to NM_207410.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:55216327 A>G maps to NM_207410.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:55264051 G>T maps to NM_207410.2 G343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:55264068 C>T maps to NM_207410.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr6:55264164 A>G did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:30544211 C>G maps to NM_024051.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr2:85780513 G>A maps to NM_000821.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:38877211 G>A maps to NM_152657.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:34912987 G>C maps to NM_024835.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr22:25007071 G>A maps to NM_005265.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:24629878 G>A maps to NM_001099781.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr22:24620981 G>A maps to NM_001099781.1 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:33442667 G>A maps to NM_178026.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr20:33450710 C>A maps to NM_178026.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr20:23967092 G>T maps to NM_178311.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr22:22989254 G>T maps to ENST00000215938 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:61995182 G>A maps to NM_000515.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr17:61958284 C>A maps to NM_002059.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:61958387 C>A did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:61958796 G>A maps to NM_002059.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr5:42695030 A>G maps to NM_000163.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:42718769 C>T maps to NM_000163.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr5:42695075 G>T maps to NM_000163.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:31011576 G>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr7:31018816 G>A maps to NM_000823.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:10331777 G>A maps to NM_016362.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:172165996 C>A maps to NM_198407.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:172166131 G>A maps to NM_198407.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:172166128 G>A maps to NM_198407.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:59611376 G>T maps to NM_005142.2 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:150417935 C>T maps to NM_130759.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr7:150417442 G>T maps to NM_130759.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr7:150269349 C>T maps to ENST00000430830 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr7:150269976 A>G maps to ENST00000430830 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr7:150324860 G>T maps to ENST00000438845 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:150325055 G>A maps to ENST00000438845 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:150217667 T>A maps to NM_153236.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:150217086 C>T maps to NM_153236.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr7:150174630 T>A maps to NM_175571.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:150174192 T>A maps to NM_175571.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr7:150164376 A>T maps to NM_175571.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:102440246 G>A maps to NM_017676.2 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr8:41397201 G>A maps to NM_032336.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr19:14589275 G>A maps to NM_202470.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:78511861 C>A maps to NM_017655.4 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr19:46181222 G>A maps to NM_000164.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:110376234 G>T maps to NM_057169.3 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:121768133 T>C maps to NM_000165.3 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:121768671 G>T maps to NM_000165.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:121768434 C>T maps to NM_000165.3 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:90605194 C>T maps to NM_032602.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr6:90604279 C>T maps to NM_032602.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr1:147230637 G>A maps to NM_005266.5 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:147380453 G>T maps to NM_005267.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:147380118 G>T maps to NM_005267.4 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr13:20763462 C>A maps to NM_004004.5 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:35250800 C>G maps to NM_001005752.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:35223425 C>T maps to NM_005268.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:42883086 G>A maps to NM_001080383.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:228345524 C>T maps to NM_020435.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr15:35044939 G>T maps to NM_020660.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr15:35045122 C>A maps to NM_020660.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr15:35044962 A>G maps to NM_020660.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:30739015 G>A did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr23:30695508 C>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:30737552 G>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:30719000 A>G did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr4:80328220 C>G maps to NM_033214.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr4:80329327 C>A maps to NM_033214.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:141900353 C>A maps to NM_001039547.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:100653446 T>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:100656648 T>C did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:33109728 G>A maps to NM_000404.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:220103843 C>T maps to NM_024506.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr11:134244882 G>A maps to NM_138342.3 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:134229018 G>A maps to NM_138342.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:134212646 G>T did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:134181038 G>A maps to NM_001080407.2 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:134180991 C>A maps to NM_001080407.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr7:8095088 A>G maps to NM_138426.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:8099835 G>A maps to NM_138426.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:8125921 A>T maps to NM_138426.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr9:6604778 C>T maps to NM_000170.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:51696578 T>C maps to NM_181789.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr15:51676069 T>C maps to NM_181789.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr16:74497377 C>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr16:74499644 G>A maps to NM_012201.5 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr16:74487199 G>A maps to NM_012201.5 A1135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr12:57864775 G>T maps to NM_005269.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:57863407 C>T maps to NM_005269.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:57857554 C>A maps to NM_005269.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr12:57864529 G>T maps to NM_005269.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:57857803 C>A maps to NM_005269.2 C41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:121708905 C>T maps to NM_005270.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr7:42011971 G>A maps to NM_000168.5 C689C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr7:42005901 G>A maps to NM_000168.5 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:42005724 C>A maps to NM_000168.5 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:42065845 C>A maps to NM_000168.5 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:42005484 C>T maps to NM_000168.5 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:42004164 T>A maps to NM_000168.5 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:75804236 G>A maps to ENST00000378692 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr16:4385312 G>T maps to NM_032575.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr9:4117992 G>A maps to NM_001042413.1 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:48624359 G>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr6:39046731 G>A did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:9792886 T>G maps to NM_004246.1 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:14625262 G>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:14550467 A>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:14599311 G>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:14748526 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:14708971 G>T did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:14550410 A>T did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr4:175565116 G>A maps to NM_006529.2 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:102974191 G>C did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:102962290 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:102962375 C>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:102974009 G>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:102974155 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:102977156 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:131959236 G>T maps to NM_006541.4 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:191760376 G>A maps to NM_014905.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:129431904 G>T maps to ENST00000442111 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:17691561 C>T maps to NM_024656.2 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:17692172 C>T maps to NM_024656.2 Q597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:183944265 G>T maps to NM_015101.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:183942788 C>G maps to NM_015101.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:183933095 C>T maps to NM_015101.2 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:183907945 G>A maps to NM_015101.2 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr12:104390536 G>A maps to NM_031302.3 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:1263142 G>C maps to NM_001029885.1 *215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:48204586 G>T maps to NM_015711.3 E1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr10:88834323 T>G maps to NM_005271.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr23:120181665 C>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:120182742 C>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:120181838 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:120183011 G>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:120181846 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:120181735 C>G did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:120182951 G>C did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:120182718 C>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:120181717 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:120182459 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:58715438 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:58722699 C>A maps to NM_080661.2 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:4863803 G>A maps to NM_032569.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr16:4871571 C>T maps to NM_032569.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr19:19752823 T>C maps to NM_016573.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:16290708 T>C maps to NM_006877.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr3:155654154 G>T maps to NM_003875.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:63010557 G>A maps to NM_006572.4 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr9:80537166 C>T maps to NM_002072.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr20:57474004 A>G maps to NM_080425.2 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr20:57428682 T>G maps to NM_080425.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr20:57415388 C>T maps to NM_016592.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr20:57415202 C>A maps to NM_016592.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr20:57484237 G>A maps to NM_080425.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:110148994 G>C maps to NM_005272.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:80108230 C>T maps to NM_001102386.1 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:6954922 C>T maps to NM_002075.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:6952793 A>T did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr12:6952168 G>A maps to NM_002075.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:36227384 C>A maps to NM_001128227.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:68171222 C>A maps to NM_018841.5 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:93536069 C>T maps to NM_021955.3 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr6:30514614 T>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:30515027 G>A maps to NM_005275.3 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr3:52724611 G>T maps to NM_014366.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:54565512 G>C did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:54565500 G>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:54565512 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:54578750 C>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:54581037 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:54569758 G>T did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:44705118 G>A maps to NM_138335.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:44713027 G>C maps to NM_138335.1 S179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr12:102155096 T>C maps to NM_024312.4 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr12:102161812 A>G did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr12:102158640 G>C maps to NM_024312.4 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr16:1412531 C>A maps to NM_032520.4 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:65113899 G>T maps to ENST00000418919 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:131021484 C>T maps to NM_004486.4 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:100551469 T>A maps to ENST00000266746 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:133357409 C>A maps to NM_005895.3 E1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:133373126 G>A maps to NM_005895.3 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:37366071 C>T maps to NM_001172713.1 Q921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr3:37292887 G>T maps to NM_001172713.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:93273304 G>T maps to NM_005113.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:74372959 C>T maps to NM_001038640.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:74364585 T>C maps to NM_001038640.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr15:74365124 G>A maps to NM_001038640.2 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:121396220 G>A maps to ENST00000393667 Q2984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:121414946 C>A maps to ENST00000393667 E1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:121410335 G>T maps to ENST00000393667 A2625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:121417434 C>A maps to ENST00000393667 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr3:167758632 C>A maps to NM_014498.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:167750307 C>T maps to NM_014498.3 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:167747049 G>A maps to NM_014498.3 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr9:88655733 G>T maps to ENST00000376023 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:150634404 C>A did not map to a codon.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr1:155764900 C>A maps to ENST00000368331 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:155730293 G>A maps to ENST00000368331 Q1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:155823172 T>C maps to ENST00000368331 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:117896344 T>G maps to NM_020399.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:101190259 G>T maps to NM_002079.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr16:20335150 C>A maps to NM_001007240.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr16:20331588 G>A maps to NM_001007240.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:194118279 G>A maps to NM_004488.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:194118432 C>T maps to NM_004488.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:167038336 G>A maps to NM_005814.1 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr8:145138687 C>G maps to NM_003801.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:145140221 C>T maps to NM_003801.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr10:113915649 G>T maps to NM_020918.4 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr10:113924308 C>T maps to NM_020918.4 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr10:113928282 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:27226882 C>T maps to NM_022078.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:156568033 T>A maps to NM_015590.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:42478424 G>A maps to NM_001002909.2 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:42513911 C>T maps to NM_001002909.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:42478508 G>T maps to NM_001002909.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr1:46099320 T>A did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:46106067 C>A maps to NM_021639.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:46093978 T>A maps to NM_021639.4 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:241398477 C>A maps to NM_002081.2 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:99774749 C>A maps to NM_152742.1 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:132888122 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:132834023 G>T did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:133087078 T>G did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:132887630 C>A did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:132887884 A>G did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:132887888 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:132795840 G>A did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:132437086 A>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:132458414 G>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr20:5554611 C>T maps to NM_019593.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr2:157425353 C>T maps to NM_000408.4 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:63784446 C>T maps to ENST00000314140 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr14:63784563 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr14:67588970 A>G did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr14:67555742 C>T maps to NM_020806.4 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:34869910 G>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:34890128 C>T maps to NM_000175.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:48973957 T>C did not map to a codon.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:24448430 G>A maps to NM_001503.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:176594914 C>A maps to NM_005277.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr4:176622805 C>T maps to NM_005277.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:27858011 C>T maps to NM_007266.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:27861079 C>T maps to NM_007266.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr2:27855501 G>A maps to NM_007266.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:27852009 G>T maps to NM_007266.3 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:110893648 C>G maps to NM_001164373.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:23296640 C>T maps to ENST00000435486 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:136112438 G>T did not map to a codon.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:46977382 G>A maps to ENST00000283297 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr6:46977154 G>A maps to ENST00000283297 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:135427977 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:135496411 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:135428120 T>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:135474459 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:135431463 G>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:135429394 T>C did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:135431137 G>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:135428801 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:135428577 G>C did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:135432347 T>C did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:135429361 C>A did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:135441477 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:135443705 A>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:135432362 T>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:135405369 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:135405391 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:135430017 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:135496474 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:135429071 G>T did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:135430460 C>A did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:135429118 T>G did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:26534384 C>T maps to NM_001145168.1 Q737Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:47682287 C>A maps to NM_153838.3 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:47682588 C>A maps to NM_153838.3 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:47682681 C>T maps to NM_153838.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:46826468 G>A maps to NM_015234.4 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:46826654 G>A maps to NM_015234.4 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr6:46826156 G>A maps to NM_015234.4 V1161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:46826855 G>A maps to NM_015234.4 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:46828475 G>C maps to NM_015234.4 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:27333079 G>A maps to NM_005288.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr13:27333754 G>A maps to NM_005288.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:95347065 C>G maps to NM_181745.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr8:37696508 C>A maps to NM_032777.9 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr8:37672476 G>T maps to NM_032777.9 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr8:37699011 C>T maps to NM_032777.9 C1052C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr8:37686462 G>A maps to NM_032777.9 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr4:22414849 G>A maps to NM_145290.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr4:22390766 G>A maps to NM_145290.2 C889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr4:22389780 G>A maps to NM_145290.2 H1171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr4:22390724 C>T maps to NM_145290.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:142764489 C>T maps to NM_198569.2 D1197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:100373723 C>T maps to NM_032787.2 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr3:100378606 C>A maps to NM_032787.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:100365480 G>A maps to NM_032787.2 W393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:100362184 G>A maps to NM_032787.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:105517537 C>T maps to NM_013345.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:105518188 C>A maps to NM_013345.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr14:105518035 G>T maps to NM_013345.2 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:131590382 C>T maps to NM_198827.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr12:131569198 C>G maps to NM_198827.3 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:37780664 C>T maps to NM_181791.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:72368027 G>T maps to ENST00000440684 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:72368180 G>T maps to ENST00000440684 R1240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:9728818 C>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:9728765 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:9728758 C>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:131486963 G>A maps to NM_207364.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:131487617 A>G maps to NM_207364.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:131487665 C>T maps to NM_207364.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:154055652 G>T maps to NM_001038705.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:154055875 G>C maps to NM_001038705.1 S603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:154147143 G>T maps to NM_001038705.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:98251938 G>A maps to NM_005290.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:98251485 C>A maps to NM_005290.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr3:98251899 C>G maps to NM_005290.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr5:145895655 T>C maps to NM_194251.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:67220114 G>A maps to NM_206997.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:67219031 G>A maps to NM_206997.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:6314830 C>G maps to NM_207370.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:119900053 C>T maps to NM_153002.2 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:119886043 C>A maps to NM_153002.2 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr10:25888199 G>T maps to NM_020752.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr10:25878044 C>A maps to NM_020752.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr10:25887461 G>A maps to NM_020752.2 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr10:25887112 C>A maps to NM_020752.2 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr10:25877957 G>A maps to NM_020752.2 W592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr10:25887944 G>A maps to NM_020752.2 E1130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:169802047 A>T maps to NM_014373.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:168059877 C>T maps to NM_153832.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:168056835 C>A maps to NM_153832.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:6933861 C>A maps to NM_019858.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:128408677 C>T maps to NM_005291.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:145584560 C>T maps to NM_024531.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:53105979 C>T did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr23:53106310 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:53105955 T>C did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:53106693 C>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:78426663 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:78427454 A>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:78427295 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:78426581 C>G did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:40094102 G>T maps to NM_007223.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr15:40094082 G>A maps to NM_007223.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:36499257 C>A maps to ENST00000398597 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr13:99907652 C>G maps to NM_005292.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr12:57390015 G>A maps to NM_007264.3 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr13:99948237 G>A maps to NM_004951.4 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr7:107115494 T>A maps to NM_005295.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:167571220 C>A maps to NM_005299.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:167570776 G>C maps to NM_005299.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:51274369 C>T maps to NM_001506.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:51274864 G>A maps to NM_001506.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:41555558 G>T did not map to a codon.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr7:124387340 G>A maps to NM_005302.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr7:124386656 G>T maps to NM_005302.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:124404584 G>C maps to NM_005302.2 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:124386947 G>A maps to NM_005302.2 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:133402692 G>A maps to NM_001508.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:46094287 A>G maps to NM_005282.2 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:46094365 G>T maps to NM_005282.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr2:105859091 G>A maps to NM_007227.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:150349045 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:150348606 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:150349888 C>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:150345262 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:150349093 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:174417515 C>T maps to NM_005684.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:174417423 C>T maps to NM_005684.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:231774969 C>A maps to NM_005683.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr2:231775188 C>A maps to NM_005683.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:231775272 G>T maps to NM_005683.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:57695776 G>T maps to NM_005682.5 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:57685307 C>G maps to NM_005682.5 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:110301088 G>A maps to ENST00000414000 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:97247580 C>A maps to NM_030784.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:97246935 G>A maps to NM_030784.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:19025355 G>T did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:19021037 A>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:19025394 T>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:19024150 C>G did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:19021156 G>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:19013117 T>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:19018071 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:19028828 G>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:88477619 C>A maps to NM_003608.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:91700653 C>T maps to ENST00000238699 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:54081849 G>T maps to NM_006794.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr19:47844850 C>A maps to NM_018485.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr4:8588915 C>T maps to NM_080819.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:94134044 G>C maps to NM_016540.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:94113827 G>T maps to NM_016540.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:151012965 G>C maps to NM_023915.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:151012302 G>C maps to NM_023915.3 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:147408772 C>T maps to NM_016334.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:89989704 A>T did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr5:89921056 C>T maps to NM_032119.3 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:89981777 G>A maps to NM_032119.3 V2152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr5:90015975 C>T maps to NM_032119.3 L3187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:89992781 C>A maps to NM_032119.3 T2658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr5:90052866 G>T maps to NM_032119.3 R3943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:90368329 G>A maps to NM_032119.3 V6073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:90074905 C>A maps to NM_032119.3 L4358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr5:89953948 G>T maps to NM_032119.3 E1536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:101908915 G>T did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:101911508 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:101909359 G>C did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:101909537 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:101912006 C>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:101911774 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:101908954 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:101909872 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:101912634 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:101911569 G>T did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:101972176 G>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:101970928 G>C did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:101970973 G>C did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr12:13061272 C>T maps to NM_003979.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr16:19883783 G>T maps to NM_016235.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr16:19883336 C>G maps to NM_016235.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:72436966 G>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:72436490 C>T maps to NM_022036.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr6:117113451 G>C maps to NM_148963.2 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:117150011 G>T maps to NM_148963.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr4:90169134 G>T maps to NM_198281.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:109441603 C>A maps to NM_013296.4 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr16:46943684 C>T maps to NM_133443.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:46931633 C>T maps to NM_133443.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:28472237 G>T maps to NM_182701.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:53073985 A>T maps to NM_015696.4 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:35505199 C>T maps to NM_020895.3 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:123476184 C>A maps to ENST00000456860 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:113664294 G>A maps to NM_017577.4 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:113595040 C>T maps to NM_017577.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:113623040 C>A maps to NM_017577.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:125822582 C>T maps to NM_023927.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:47033852 C>T maps to NM_015124.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr22:47059979 G>A maps to NM_015124.2 W228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:47069574 G>C maps to NM_015124.2 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr22:47069653 A>T maps to NM_015124.2 K443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr7:50680467 C>A maps to NM_005311.4 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr7:50660792 G>A maps to NM_005311.4 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr7:50680467 C>A maps to NM_005311.4 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr7:50674066 C>T maps to NM_005311.4 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:165378552 C>T maps to NM_004490.2 W251*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-85-6561-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:11741048 G>A maps to NM_014668.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:11758654 G>A maps to NM_014668.3 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr15:33023382 T>A maps to NM_013372.6 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr8:102570784 C>T maps to NM_024915.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr9:37424896 C>T maps to ENST00000377824 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:153190659 G>T maps to NM_001114183.1 G866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:153030007 G>A maps to NM_001114183.1 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:158281078 G>A maps to NM_000826.3 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:158257695 G>A maps to NM_000826.3 W547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr4:158242639 C>G maps to NM_000826.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr4:158224786 G>T maps to NM_000826.3 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr4:158253996 C>T maps to NM_000826.3 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr4:158254041 A>G maps to NM_000826.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:158284165 C>T maps to NM_000826.3 N874N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr4:158224785 C>T maps to NM_000826.3 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:122598732 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:122319750 C>G did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:122387381 A>G did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:122319712 G>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:122598714 G>A did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:122532571 G>A did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr23:122528847 C>A did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:122613995 G>C did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:122532509 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:122537299 T>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:122561814 G>C did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr23:122528858 G>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:122537352 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:105623868 C>A maps to NM_000829.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:105804489 C>A maps to NM_000829.3 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:105797514 C>T maps to NM_000829.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:88123701 C>T maps to NM_017551.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr10:87489308 G>A maps to NM_017551.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr4:94690579 C>A maps to NM_001510.2 G860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:94693264 T>A maps to NM_001510.2 R880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr21:31062213 G>C maps to ENST00000327783 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr21:31023581 A>G maps to ENST00000327783 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr6:102074483 C>A maps to NM_021956.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr6:101847224 G>A maps to NM_021956.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:102503424 C>A maps to NM_021956.4 Y844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr6:102307215 C>T maps to NM_021956.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:37271861 C>G maps to NM_000831.3 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:37346263 G>T maps to NM_000831.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:37324735 G>A maps to NM_000831.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr1:37271747 C>A maps to NM_000831.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr1:37271848 C>A maps to NM_000831.3 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:120823586 C>T maps to NM_014619.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr11:120673442 C>A maps to NM_014619.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:42563518 G>A maps to NM_002088.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:42566696 G>A maps to NM_002088.3 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:42557752 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:9934561 C>T maps to NM_000833.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr16:9857425 G>A maps to NM_000833.3 Y1325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:9857191 C>G maps to NM_000833.3 S1403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:9857083 G>T maps to NM_000833.3 Y1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:9923492 A>C maps to NM_000833.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr16:9858400 C>T maps to NM_000833.3 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr16:9862767 C>A maps to NM_000833.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:13720177 T>C maps to NM_000834.3 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:14018919 C>A maps to NM_000834.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr12:13768054 G>T maps to NM_000834.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:13716390 G>A maps to NM_000834.3 Q1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr12:13768105 T>A maps to NM_000834.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr12:13716958 C>T maps to NM_000834.3 G1071G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:13716469 C>T maps to NM_000834.3 S1234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr12:13716346 G>A maps to NM_000834.3 N1275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:13720030 G>A maps to NM_000834.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:13716970 G>A maps to NM_000834.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:72840420 G>A maps to NM_000835.3 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr17:72842295 G>C maps to NM_000835.3 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr17:72846476 G>A maps to NM_000835.3 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:48945181 C>T maps to NM_000836.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr19:48922941 C>G maps to NM_000836.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr9:104390664 C>A maps to NM_133445.2 G791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:104432716 G>A maps to NM_133445.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr9:104432781 G>T maps to NM_133445.2 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr19:1004633 G>A maps to NM_138690.1 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr8:145066864 C>T maps to NM_001009184.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:66849291 C>G maps to ENST00000359742 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:48837631 C>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:48853674 G>C did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:48849875 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:48858605 C>T did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr4:3029675 G>A maps to NM_182982.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:121182679 C>T maps to NM_005308.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr3:141497222 C>A maps to NM_139209.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr19:47423516 C>T maps to NM_004491.4 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:47422550 G>T maps to NM_004491.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:47422076 G>T maps to NM_004491.4 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:47423194 G>A maps to NM_004491.4 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:146480688 C>T maps to NM_000838.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr6:146480697 C>A maps to NM_000838.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr6:146755508 C>A maps to NM_000838.3 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:51746553 G>T maps to NM_000839.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr7:86468971 C>T maps to NM_000840.2 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:86415830 C>T maps to NM_000840.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr7:86416061 C>A maps to NM_000840.2 Y318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:86415632 C>T maps to NM_000840.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:86394892 G>T maps to NM_000840.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr7:86493635 C>A maps to NM_000840.2 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:86468857 C>T maps to NM_000840.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr6:34004260 G>A maps to NM_000841.1 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr6:34004041 C>A maps to NM_000841.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr6:34008083 T>A maps to NM_000841.1 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:88386498 C>T maps to NM_001143831.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:88337889 C>A maps to NM_001143831.2 G464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr11:88300726 G>T maps to NM_001143831.2 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:88300888 G>C maps to NM_001143831.2 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:88242497 T>C maps to NM_001143831.2 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:88780920 G>C maps to NM_001143831.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr5:178413280 G>T maps to NM_000843.3 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:178413424 G>T maps to NM_000843.3 Y610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr5:178410090 G>T maps to NM_000843.3 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr5:178410090 G>A maps to NM_000843.3 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:178416113 G>A maps to NM_000843.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr3:7620395 G>A maps to NM_181874.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:7188171 G>T maps to NM_181874.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:126173068 G>A maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:126173392 C>T maps to NM_001127323.1 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr7:126173377 C>G maps to NM_001127323.1 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:126173614 G>A maps to NM_001127323.1 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr7:126544699 A>G maps to NM_001127323.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:126173011 T>A maps to NM_001127323.1 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:126249442 G>T maps to NM_001127323.1 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr17:42429093 C>T maps to NM_002087.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr18:56892921 C>A maps to NM_002091.3 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:148730656 G>T maps to NM_152407.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:16170712 C>G did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:16170750 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:16170571 T>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:16170734 C>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr4:71698952 A>G maps to NM_002092.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr4:71698084 C>T maps to NM_002092.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:48949682 G>T maps to NM_031485.3 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:42895558 T>C maps to NM_001080476.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr4:42895357 T>C maps to NM_001080476.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:42895621 G>T maps to NM_001080476.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr17:38068664 T>C maps to NM_001165958.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr17:38073395 C>T maps to NM_001165958.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:38073398 G>T maps to NM_001165958.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:144644649 G>T maps to NM_024736.6 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:144644929 G>A maps to NM_024736.6 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr12:13243686 T>C maps to NM_001080555.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr16:27818806 C>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr16:27802691 C>A maps to NM_001109763.1 *332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr19:42740844 C>A maps to NM_019884.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:42740861 C>A maps to NM_019884.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:119562179 G>A maps to NM_002093.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr9:124064368 G>A maps to NM_000177.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr16:11979112 T>C maps to NM_002094.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:51487831 G>T did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:51488590 G>A did not map to a codon.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr23:51487662 C>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr8:30557629 G>A maps to NM_000637.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:52659011 G>A maps to NM_145740.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:52661109 C>A maps to NM_145740.3 G48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr4:106647743 C>A maps to NM_001031720.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:110255768 G>T maps to ENST00000369812 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:110260012 T>C maps to ENST00000369812 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr22:24323193 G>T maps to NM_000854.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:144903179 C>T maps to NM_001164629.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:144899606 C>G maps to NM_001164629.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:144903214 C>A maps to NM_001164629.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr14:81670325 G>A maps to NM_015859.2 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:48873631 G>A maps to NM_172311.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:48898755 T>A maps to NM_172311.2 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr3:120469461 G>A maps to NM_005513.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr8:30469974 A>G maps to NM_002095.4 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr6:30876829 C>A maps to NM_001517.4 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr6:30881677 C>A maps to NM_001517.4 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:73969721 G>C did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr7:73969795 C>T maps to NM_016328.2 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr16:27495560 G>A maps to NM_001520.3 V1324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr16:27497326 G>T maps to NM_001520.3 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:27497347 G>A maps to NM_001520.3 C1276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:27503960 C>A maps to NM_001520.3 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr16:27518416 C>A maps to NM_001520.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:197631414 G>A maps to NM_012086.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr9:135553824 T>C maps to NM_012204.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr22:39122019 G>T maps to NM_004286.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:43592736 G>A maps to NM_019096.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:17449959 G>T maps to NM_133644.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr10:1053022 G>T maps to NM_012341.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr20:42355043 G>T maps to NM_176791.3 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr6:42141462 G>T maps to NM_000409.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:106681205 T>C did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:106810215 A>T maps to ENST00000282249 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr4:156631982 T>C maps to NM_001130684.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr4:156632318 G>T maps to NM_001130684.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr4:156651262 C>T maps to NM_001130684.1 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr12:14849358 C>T maps to NM_004963.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr12:14766077 G>T maps to NM_004963.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:14796592 C>G maps to NM_004963.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:14778781 G>T maps to NM_004963.3 R773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr17:7907006 C>A maps to NM_000180.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:108635313 G>C did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:108619383 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:108636236 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:108719022 A>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:108619186 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:108619152 C>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:108625391 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:108719117 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:108636212 A>G did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:108684579 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:228334601 G>T maps to ENST00000366720 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr7:65429348 C>A maps to NM_000181.3 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:65444482 G>A maps to NM_000181.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr3:72971410 C>T maps to NM_001080393.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:2778074 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:2795307 C>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:2773035 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:2773120 G>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:145038081 G>C maps to NM_002099.6 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:127447885 A>C maps to NM_002101.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:49474214 C>A maps to NM_002103.4 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:49489217 G>A maps to NM_002103.4 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:21715932 G>A maps to NM_021957.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr12:21712601 G>C maps to NM_021957.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:21693478 A>T maps to NM_021957.3 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:21711178 G>A maps to NM_021957.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:23345384 C>G maps to NM_022482.3 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:54404138 C>T maps to NM_006144.3 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:25102257 G>A maps to ENST00000382542 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr7:44874123 C>T maps to ENST00000421098 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:71860027 C>T maps to NM_018649.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr23:103267885 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:103267932 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:103268109 C>A did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:31944860 A>G maps to NM_001013699.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:31944971 A>G maps to NM_001013699.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:31945070 T>C maps to NM_001013699.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:9323659 C>A maps to NM_004285.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:9324426 A>T maps to NM_004285.3 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:115341887 C>A maps to NM_004132.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:99228024 T>C maps to NM_014282.2 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:105233140 T>A maps to NM_020771.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:26462000 G>T maps to NM_000182.4 C26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:26418041 C>G maps to NM_000182.4 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:26424189 C>G did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:26501539 G>A maps to NM_000183.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr16:777523 C>T maps to NM_207112.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:7866511 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr20:7894953 G>T maps to NM_017545.2 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:82948290 C>A maps to NM_001884.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:156594435 C>A maps to NM_021817.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr15:89421335 C>T maps to NM_178232.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr15:89424921 T>A maps to NM_178232.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr5:140056475 G>T maps to NM_002109.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:140056259 G>T maps to NM_002109.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140075749 C>T maps to NM_012208.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:52219606 A>T maps to NM_001523.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:52217093 C>A maps to NM_001523.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr8:122641415 T>C maps to NM_005328.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr8:122641064 C>T maps to NM_005328.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr2:172844236 C>G maps to NM_003642.3 Y351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:172822352 C>T maps to NM_003642.3 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:2241767 G>A maps to NM_024511.5 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr9:19063105 G>C maps to NM_017645.3 S510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:17169360 G>A maps to NM_033417.1 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:156479624 G>C maps to NM_001173393.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:156535958 C>A maps to NM_032782.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:156533929 G>A maps to NM_032782.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr16:227340 T>C maps to NM_000558.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:5289728 G>C maps to NM_005330.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:5290707 C>A maps to NM_005330.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:135287502 G>A maps to NM_006620.3 Y669Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:11133043 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:153220572 T>A did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr12:104487211 G>T maps to NM_013320.2 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr3:121363747 C>A maps to NM_005335.4 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:121350948 T>A maps to NM_005335.4 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:45267353 C>T maps to NM_021072.2 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:45262235 C>G maps to NM_021072.2 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr5:45462028 G>A maps to NM_021072.2 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr5:45645700 C>T maps to NM_021072.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr5:45267347 G>T maps to NM_021072.2 C542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:45262787 G>T maps to NM_021072.2 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr5:45262583 G>T maps to NM_021072.2 C704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr5:45353288 C>T maps to NM_021072.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:45645430 G>T maps to NM_021072.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr5:45396629 C>T maps to NM_021072.2 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr5:45262685 C>A maps to NM_021072.2 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:45353207 C>T maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr5:45396617 A>G maps to NM_021072.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:45262352 C>T maps to NM_021072.2 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:45262721 G>C maps to NM_021072.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:45267205 G>A maps to NM_021072.2 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:45462082 G>A maps to NM_021072.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr5:45262825 G>A maps to NM_021072.2 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:155252471 G>T maps to NM_020897.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr6:55128621 T>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr6:55128571 C>G maps to NM_001526.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr5:141005609 C>A maps to NM_003883.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr2:239975205 C>T maps to NM_006037.3 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:239988489 G>A maps to NM_006037.3 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:239990257 C>A maps to NM_006037.3 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:240016747 C>T maps to NM_006037.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:48185722 C>G maps to NM_015401.3 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:71708786 C>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr7:18869171 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:18705918 G>C maps to NM_178425.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr15:50549708 G>A maps to NM_002112.3 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:6995376 T>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:242192393 G>C maps to NM_005336.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:242192405 G>A maps to NM_005336.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:83724270 G>A did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr23:83723532 G>C did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:83723683 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:83724451 G>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:83723922 C>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:83724490 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:83724374 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:236727824 G>C maps to NM_018072.5 L1524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:236746379 C>G maps to NM_018072.5 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:796504 C>A maps to NM_017802.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:37230715 C>T maps to NM_019024.1 Q1673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:37215787 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:37247017 C>A maps to NM_019024.1 V1346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:37255255 C>T maps to NM_019024.1 E1221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:37283722 C>A maps to NM_019024.1 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:37229650 G>C maps to NM_019024.1 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:37241160 T>A maps to NM_019024.1 V1369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr8:145278048 C>T maps to NM_032450.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:41032872 C>T maps to ENST00000296803 W805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:41000863 C>T maps to ENST00000296803 W1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:41057274 G>T maps to ENST00000296803 C285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:41058233 G>T maps to ENST00000296803 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:41069801 A>G maps to ENST00000296803 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:41019107 A>T maps to ENST00000296803 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr5:41007489 A>T maps to ENST00000296803 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr5:41004482 C>A maps to ENST00000296803 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr5:41008871 C>A maps to ENST00000296803 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:41000934 C>A maps to ENST00000296803 E1400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr5:40998192 G>A maps to ENST00000296803 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr5:41010114 G>A maps to ENST00000296803 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:41065439 G>T maps to ENST00000296803 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:41018457 C>G maps to ENST00000296803 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:31604319 G>A maps to NM_015382.2 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr10:93244287 A>G maps to ENST00000446394 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:43506109 C>T maps to NM_015052.3 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:43594212 G>A maps to NM_015052.3 V1511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr7:43436456 A>G maps to NM_015052.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr7:43484408 C>A maps to NM_015052.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr7:43485092 C>A maps to NM_015052.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:43484985 G>T maps to NM_015052.3 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:43351582 C>A maps to NM_015052.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:43485044 G>A maps to NM_015052.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:43547725 G>T maps to NM_015052.3 E1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:197183867 T>A maps to NM_020760.1 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:197184219 G>C maps to NM_020760.1 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr2:197208379 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:197171250 G>A maps to NM_020760.1 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:197194299 T>A maps to NM_020760.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:197085592 C>A maps to NM_020760.1 E1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:124720846 G>A maps to NM_020733.1 N1122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr3:124746085 C>T maps to NM_020733.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:124720846 G>A maps to NM_020733.1 N1122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:66700231 G>T maps to NM_033647.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr12:66725229 C>T maps to NM_033647.2 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:84376792 G>A maps to NM_133636.2 N18N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:84374924 G>C maps to NM_133636.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:185941589 G>A maps to NM_001029887.1 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr4:185940563 G>C maps to NM_001029887.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr17:65156378 G>C maps to NM_014877.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:100692959 G>T maps to NM_018437.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr9:100693231 C>A maps to NM_018437.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr3:50617289 G>T maps to NM_016173.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:92848546 G>T maps to ENST00000453812 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr7:92838130 A>G maps to ENST00000453812 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:92848754 G>T maps to ENST00000453812 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:65417677 G>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:65480021 T>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:65393452 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:65409664 T>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:65476031 G>A did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:65414987 A>G did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:65409595 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:65423208 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:65423282 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:65476118 C>G did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:65392408 C>G did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:65427121 A>G did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:65427157 G>T did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:65420452 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:65408292 C>A did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:65486439 C>G did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:65427993 T>A did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:65412099 C>A did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:65417697 G>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:65474969 T>G did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:65423335 T>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:93803538 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:93837755 G>A maps to NM_001098672.1 K915K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:93844933 C>A maps to NM_001098672.1 I1118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr11:93822053 C>A maps to NM_001098672.1 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:63922664 C>T maps to ENST00000261887 Q4322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:64010801 G>A maps to ENST00000261887 Q1317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:64027021 T>C maps to ENST00000261887 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr15:64048841 G>A maps to ENST00000261887 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr15:63929829 G>A maps to ENST00000261887 Q4036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:28386601 G>A maps to NM_004667.4 L3997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:28391398 G>A maps to NM_004667.4 I3664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr15:28370264 G>T maps to NM_004667.4 R4293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr15:28491924 G>A maps to NM_004667.4 F1118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:28493708 G>C maps to NM_004667.4 S1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr15:28483880 C>T maps to NM_004667.4 E1205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr15:28518104 G>T maps to NM_004667.4 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:28460910 C>G maps to NM_004667.4 R2022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr15:28380781 C>T maps to NM_004667.4 S4024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:28386673 G>C maps to NM_004667.4 V3973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:89591351 C>T maps to NM_014606.1 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr4:89526979 A>G maps to NM_014606.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr4:89574023 C>G maps to NM_014606.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr4:89591399 G>T maps to NM_014606.1 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr4:89385003 A>G did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:89400576 C>A maps to NM_016323.2 C552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:89427027 G>T maps to NM_016323.2 *1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:89358062 G>A maps to NM_017912.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr4:89363383 A>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr7:35673300 C>A maps to NM_022373.4 *407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr15:72643536 C>T maps to ENST00000457859 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr8:80677842 C>A maps to NM_001040708.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:40092475 C>A maps to NM_014571.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr6:26091105 A>G maps to NM_000410.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:91843988 G>A maps to NM_001017975.3 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:91781508 C>T maps to NM_001017975.3 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:91859729 A>T maps to NM_001017975.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:91740342 A>G maps to NM_001017975.3 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:120357314 A>C maps to NM_000187.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:81392129 G>A maps to NM_000601.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr7:81350119 G>C maps to NM_000601.4 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:81350086 C>T maps to NM_000601.4 W415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:43033219 T>C maps to ENST00000458501 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:42738545 C>T maps to NM_020707.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:145629325 C>T maps to NM_022475.1 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:222712087 G>A maps to NM_024746.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:222716922 C>T maps to NM_024746.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr1:222715354 T>A maps to NM_024746.3 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr3:108072394 C>T maps to NM_007072.2 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr9:97207433 G>A maps to NM_032558.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:1961105 C>T maps to NM_001098202.1 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:21799209 G>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr22:21800818 C>T maps to NM_015094.2 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr22:21800554 C>T maps to NM_015094.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:46807268 C>G maps to NM_152795.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:46811548 G>C maps to NM_152795.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:46811521 T>A maps to NM_152795.2 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:42926620 G>A did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr9:35813518 G>A maps to NM_032593.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:75171273 C>A maps to NM_005338.4 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr7:75228544 G>A maps to NM_005338.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:114499409 T>G maps to ENST00000426820 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:114483935 C>T maps to ENST00000426820 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr7:139305194 G>A maps to NM_022740.4 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr7:139257805 G>T maps to NM_022740.4 S1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr19:40886742 G>A maps to NM_144685.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr22:19371174 G>T maps to NM_003325.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr22:19384471 T>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:19371183 C>T maps to NM_003325.3 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:19384324 G>C maps to NM_003325.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:30004864 T>G maps to NM_003609.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:27835169 C>G maps to NM_005322.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr6:27835193 C>A maps to NM_005322.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:26056650 G>A maps to NM_005319.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr6:26056215 C>T maps to NM_005319.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:26056116 C>T maps to NM_005319.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr6:26234507 C>T maps to NM_005320.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:26234617 G>A maps to NM_005320.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr6:26234963 C>T maps to NM_005320.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr6:26157146 A>T maps to NM_005321.2 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:26157145 G>T maps to NM_005321.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr6:26033763 A>C maps to NM_003513.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr6:26199404 C>A maps to NM_021065.2 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr6:27101011 G>A maps to NM_021064.4 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr6:27115230 C>T maps to NM_080596.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr6:26123910 G>A maps to NM_003526.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:26158468 G>A maps to NM_138720.1 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:26158771 C>A maps to NM_138720.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:26200139 C>A maps to NM_003522.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr6:27100229 G>A maps to NM_021058.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr6:27114543 T>A maps to NM_080593.2 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr6:27114418 G>A maps to NM_080593.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr6:27806768 C>T maps to NM_003520.3 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:26020743 G>T maps to NM_003529.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:26197079 C>G maps to NM_003530.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr6:26197190 G>T maps to NM_003530.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr6:26225531 C>G maps to NM_003532.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:26225435 C>A maps to NM_003532.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr6:26250686 G>A maps to NM_021018.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr6:26271446 G>A maps to NM_003534.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:27839937 G>A maps to NM_003533.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:26205084 G>A maps to NM_003545.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:27841216 G>A maps to NM_003546.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:27841264 C>G maps to NM_003546.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:149859298 G>C maps to NM_175065.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:149858023 G>T maps to NM_003528.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:149858142 C>T maps to NM_003528.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:149783692 G>T maps to ENST00000427880 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:149783656 G>A maps to ENST00000427880 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:149783773 C>T maps to ENST00000427880 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:149785212 G>A maps to NM_001123375.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:12124482 G>A maps to NM_002114.2 Q1485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr6:12163562 C>T maps to NM_002114.2 P2342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr6:12124416 A>G maps to NM_002114.2 P1463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:143090844 G>T maps to NM_006734.3 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:143094042 A>G maps to NM_006734.3 H611H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr6:143092296 T>C maps to NM_006734.3 Q1193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:42047564 G>C maps to NM_024503.3 P968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:42048313 T>A maps to NM_024503.3 K719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:42045797 C>T maps to NM_024503.3 K1557K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:42048059 G>A maps to NM_024503.3 T803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr1:42049198 G>A maps to NM_024503.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr10:71158371 G>A maps to ENST00000439900 Q834Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr5:176314653 C>A maps to NM_002115.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr10:71005858 G>T maps to NM_025130.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr19:37853644 G>C maps to NM_181786.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:29911086 C>A maps to ENST00000376806 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:29911897 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:29911977 C>A maps to ENST00000376806 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:29912171 G>A maps to ENST00000376806 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:29912275 G>C did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr6:29911962 G>A maps to ENST00000376806 W228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr6:32905233 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr6:32905204 G>T maps to NM_002118.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:32905189 C>A maps to NM_002118.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:32610019 G>T maps to NM_002122.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr6:32609222 G>A maps to NM_002122.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:32713838 G>T maps to NM_020056.4 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr6:32714032 C>T maps to NM_020056.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:32549333 T>A maps to NM_002124.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr6:30459172 C>T maps to NM_005516.5 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr21:38311130 C>T did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr21:38309156 A>T maps to NM_000411.5 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:53345448 T>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr3:148786122 C>T did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr3:148789183 C>T maps to NM_003071.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:221053251 C>A maps to NM_021958.3 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:221055662 G>A maps to NM_021958.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr8:28827925 A>G maps to ENST00000444075 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:185959423 G>T maps to NM_031935.2 G1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:186039828 C>T maps to NM_031935.2 T2693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr1:186106961 T>C maps to NM_031935.2 L4594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:186031076 C>T maps to NM_031935.2 I2469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:186157124 C>A maps to NM_031935.2 R5509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:185939522 T>C maps to NM_031935.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:186088425 T>G maps to NM_031935.2 V3984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:186122916 G>T maps to NM_031935.2 G5018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:186076014 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:186010269 T>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:186147830 C>A maps to NM_031935.2 S5409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:186099717 G>C maps to NM_031935.2 V4373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr1:186072602 G>A did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr13:31036833 G>T maps to NM_002128.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:34330139 G>A maps to NM_145205.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:24143191 G>T maps to NM_000191.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:24144040 C>A maps to NM_000191.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr5:43299061 A>C maps to NM_002130.6 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr1:120295954 A>G maps to NM_005518.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:120302553 A>G maps to NM_005518.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:26801130 A>T maps to NM_005517.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr22:35660935 G>T maps to NM_001003681.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:35783129 G>A maps to NM_002133.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:173534369 C>G maps to NM_015980.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr18:61627504 T>C maps to NM_001123366.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr12:121416876 C>A maps to NM_000545.5 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:36093604 G>T maps to NM_000458.2 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:43034758 G>C maps to ENST00000338692 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr8:76463626 A>T maps to NM_004133.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:138762706 G>T maps to NM_006895.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr12:54677611 T>C maps to NM_031157.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr2:178080347 C>T maps to NM_194247.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:12907713 C>T maps to NM_001013631.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:12907843 G>T maps to NM_001013631.1 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:12907696 G>C maps to NM_001013631.1 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr4:83278593 C>A maps to NM_031370.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr10:43882165 G>A maps to NM_001098204.1 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:100667655 G>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:100668297 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr9:86585084 C>G maps to NM_031262.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr9:86591933 C>T maps to NM_031262.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:86588864 A>C maps to NM_031262.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:39330768 G>A maps to ENST00000221419 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:39329234 G>A maps to ENST00000221419 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:39330738 C>T maps to ENST00000221419 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr19:8531118 C>T maps to NM_005968.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:8550697 C>A maps to NM_005968.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:245020152 T>A maps to NM_031844.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:245027495 G>C maps to NM_031844.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:245027150 G>A maps to NM_031844.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr11:62490110 G>A maps to NM_001079559.1 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr11:62487534 C>T maps to NM_001079559.1 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr15:83561499 G>A maps to NM_199330.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:83561517 C>A maps to NM_199330.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr19:19042180 C>A maps to NM_004838.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr14:23746112 G>A maps to NM_020834.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:60325920 G>T maps to NM_015888.4 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:60314154 A>T maps to NM_015888.4 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr19:12881985 C>A maps to NM_013312.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr7:27224430 C>T maps to NM_005523.5 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:27224652 G>T maps to NM_005523.5 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:27224325 T>A maps to NM_005523.5 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:27141031 A>T maps to NM_006735.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:27148055 G>A maps to NM_153631.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:27147773 G>A maps to NM_153631.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr7:27169029 G>C maps to NM_002141.4 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr7:27169743 G>A maps to NM_002141.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr7:27170283 G>T maps to NM_002141.4 Y23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr7:27182914 G>A maps to NM_019102.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:46607015 G>T maps to NM_002144.3 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr17:46607864 C>A maps to NM_002144.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr17:46622225 C>A maps to NM_002145.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr17:46629777 G>T maps to NM_002146.4 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:46628421 C>A maps to NM_002146.4 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr17:46685368 C>A maps to NM_004502.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr17:46691645 G>A maps to NM_024016.3 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:54379714 A>G maps to NM_017409.3 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr12:54350154 C>T maps to NM_173860.1 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:54427001 G>A maps to NM_018953.2 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr12:54428080 C>A maps to NM_018953.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:54396298 G>A maps to NM_006897.1 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:176983940 C>A maps to NM_002148.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:176981714 G>T maps to NM_002148.3 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr2:176964966 G>T maps to NM_021193.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:176957926 A>C maps to NM_000523.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:177034271 A>T maps to NM_006898.4 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:177036653 G>T maps to NM_006898.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr2:177036983 C>G maps to NM_006898.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:176996058 C>T maps to NM_019558.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr4:175414318 T>C maps to NM_000860.4 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr4:95220777 G>A maps to NM_014485.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:35551593 C>T maps to NM_182983.2 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:133632688 A>G did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:100179891 C>A maps to NM_000195.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr22:26860752 G>A maps to NM_022081.4 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr11:18313247 G>A maps to NM_181507.1 C727C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:18303746 C>A maps to NM_181507.1 E1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr10:100481511 C>T maps to NM_021828.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:6452587 G>A maps to NM_000613.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr11:6453215 C>A maps to NM_000613.2 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:6453009 C>A maps to NM_000613.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:21984876 C>A maps to NM_005144.4 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:21984735 G>T maps to NM_005144.4 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:63257742 A>G maps to NM_054108.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr3:11301121 C>T maps to NM_001098211.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr3:11301421 C>A maps to NM_001098211.1 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:175110622 G>T maps to NM_001131055.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr18:22048907 C>G maps to NM_021624.3 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:152188179 G>A maps to NM_001009931.1 S1975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr1:152187705 G>T maps to NM_001009931.1 Y2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:152187516 G>T maps to NM_001009931.1 S2196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:152191643 C>A maps to NM_001009931.1 E821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr1:152187672 A>G maps to NM_001009931.1 S2144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:152191616 G>A maps to NM_001009931.1 Q830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:152188348 G>T maps to NM_001009931.1 S1919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:152187071 C>A maps to NM_001009931.1 E2345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr2:20840769 G>A maps to NM_022460.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr4:11401377 C>T maps to NM_005114.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr4:11400966 G>A maps to NM_005114.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr17:13400065 C>A maps to NM_006042.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr16:26147397 A>T maps to NM_006040.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr16:26147025 C>T maps to NM_006040.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr6:114379014 C>T maps to NM_153612.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:1961752 G>C maps to ENST00000454677 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:129026282 C>T maps to NM_004807.2 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:129026313 C>A maps to NM_004807.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:131762511 T>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr13:96743640 T>C maps to NM_153456.2 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:97485145 C>T maps to NM_153456.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr17:40705529 C>T maps to NM_000413.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:53459055 G>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:43772486 G>T maps to NM_016142.2 G63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:120057213 G>A maps to ENST00000235547 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:120050170 G>A maps to ENST00000235547 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:119965137 G>T maps to NM_000198.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:119962194 C>T maps to NM_000198.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:122720902 G>T maps to NM_004506.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:122737377 C>G maps to NM_004506.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr16:67199688 G>A maps to NM_001040667.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:56565107 C>G maps to NM_001080439.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr17:56536129 A>G maps to NM_001080439.1 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr14:102552598 C>G maps to NM_001017963.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:44217142 G>C maps to NM_007355.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:118440729 G>A maps to NM_025015.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr10:118451904 C>T maps to NM_025015.2 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr10:118451945 C>T maps to NM_025015.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr10:118434812 G>T maps to NM_025015.2 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:118460504 G>T maps to NM_025015.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:3725560 C>A maps to NM_052970.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:31779344 G>A maps to NM_005527.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr6:31778603 C>G maps to NM_005527.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr5:132406079 G>A maps to NM_002154.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr4:128725242 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:128001525 G>A maps to NM_005347.4 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:161495233 G>T maps to NM_002155.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr11:122929457 G>A maps to NM_006597.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:122931506 C>G did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr5:137895597 G>T maps to NM_004134.6 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr7:75933483 C>T maps to NM_001540.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:119617129 C>T maps to NM_014365.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr12:119617440 G>A maps to NM_014365.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr3:122496726 C>A maps to NM_024610.4 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr3:122487664 G>A maps to NM_024610.4 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:55785928 C>A maps to NM_012267.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:55776690 G>A maps to NM_012267.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:64682721 G>A did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:198358949 A>G maps to NM_199440.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:22211642 G>A maps to NM_005529.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:22155924 G>A maps to NM_005529.5 S3981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:22165441 C>T maps to NM_005529.5 R3342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:22176641 C>T maps to NM_005529.5 S2446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:22166423 C>T maps to NM_005529.5 V3200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:22181476 C>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:135593629 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:135593703 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:70921228 A>T maps to NM_002159.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:70897694 G>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:63257363 G>A maps to NM_000524.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:63257015 G>A maps to NM_000524.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:63256744 C>A maps to NM_000524.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:63257309 C>T maps to NM_000524.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:63256826 G>A maps to NM_000524.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:63256880 C>G maps to NM_000524.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:63257018 G>T maps to NM_000524.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:63256367 A>T maps to NM_000524.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr5:63256964 G>T maps to NM_000524.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:87726038 G>T maps to NM_000865.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr6:87726077 G>T maps to NM_000865.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:88040763 C>A maps to NM_000866.3 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:231973602 G>C maps to NM_000867.4 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:114141438 C>T did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr23:114141479 G>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:114082652 G>C did not map to a codon.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr23:114141491 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:114082669 C>T did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:113860283 G>T maps to NM_213621.3 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:113857403 C>T maps to NM_213621.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:113857736 C>T maps to NM_213621.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:113848604 C>A maps to NM_213621.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:113816816 C>A maps to NM_006028.3 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:113815331 C>G maps to NM_006028.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:183778073 C>T maps to NM_130770.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr3:183770894 G>A maps to NM_130770.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:183756705 C>G maps to NM_001145143.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:183822649 C>A maps to NM_182589.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:183823569 G>A maps to NM_182589.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr5:147889509 G>T maps to NM_001040173.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:154876016 G>A maps to NM_024012.2 W298*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-33-6737-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr7:154862997 G>A maps to ENST00000395731 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:154862632 C>A maps to NM_024012.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr7:154876034 C>G maps to NM_024012.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:19992590 C>G maps to NM_000871.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr10:124268200 G>A maps to NM_002775.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:8294049 C>A maps to NM_053044.3 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:3230463 C>G maps to NM_002111.6 V2657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr4:3105585 C>A maps to NM_002111.6 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:3189400 G>T maps to NM_002111.6 L1671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr21:33370926 G>T maps to NM_014586.1 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr21:33368229 G>T maps to NM_014586.1 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr21:33371223 C>T maps to NM_014586.1 H624H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr21:33371495 A>G maps to NM_014586.1 *715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr21:33296886 C>T maps to NM_014586.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr23:53581602 G>C did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:53563495 G>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:53574822 T>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:53587153 C>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:53611203 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:53574674 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:53674516 A>G did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:53578043 T>C did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:53592130 C>G did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:53578077 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:53584371 G>C did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:53573707 A>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:53596670 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:53616584 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:53610790 G>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:53641578 G>C did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:53564622 C>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:53642763 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:53634647 C>T did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:53659446 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:111099058 A>T maps to NM_001040107.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr3:50338436 C>T maps to NM_153281.1 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr3:50332931 C>T maps to NM_003549.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr7:123517196 C>T maps to NM_012269.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:123509055 G>A maps to NM_012269.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:70917871 G>A maps to NM_032821.2 V3309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:70902521 C>T maps to NM_032821.2 W3753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:70891611 G>T maps to NM_032821.2 L4096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:71098609 G>A maps to NM_032821.2 Q737*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-39-5016-01A-01D-1441-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr16:70935068 C>A maps to NM_032821.2 T2961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr16:70934959 G>A maps to NM_032821.2 L2998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:220276787 G>T did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr1:220315156 A>G maps to NM_018060.3 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:220310240 T>C maps to NM_018060.3 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr6:82924286 C>A maps to NM_015525.2 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr6:82909856 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr6:82909855 A>C did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:8272243 G>A maps to ENST00000422063 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:62081217 G>C maps to NM_001099789.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:10445844 G>T maps to NM_002162.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr20:2640343 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:153053285 C>G did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:153053587 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:39845389 G>A maps to NM_194294.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr8:39840259 G>T maps to NM_194294.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:148586590 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:6657949 G>A maps to NM_001193457.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr1:159002319 A>T maps to ENST00000295809 K390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:159021695 C>G maps to ENST00000295809 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr14:94594941 G>C maps to NM_032036.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:79120788 T>C maps to NM_006417.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:79116278 T>C maps to NM_006417.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:79101165 A>T maps to NM_006820.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:163174643 T>C maps to NM_022168.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr2:163174568 G>T maps to NM_022168.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr10:91162118 C>T maps to NM_001548.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:91099422 G>A maps to NM_001549.4 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:21206664 C>T maps to NM_002171.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr9:21367976 G>T maps to NM_006900.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:21239787 A>T maps to NM_002172.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:21227824 C>T maps to NM_021268.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr9:21305249 G>T maps to NM_002169.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr9:21350808 C>T maps to NM_021002.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr9:21409531 G>T maps to NM_002170.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr21:34625013 C>T maps to NM_207585.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr9:21481485 G>A maps to NM_176891.4 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:129226554 C>T maps to NM_052985.2 Q997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:129183504 G>A maps to NM_052985.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:129221604 G>T maps to NM_052985.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr16:1561112 G>C maps to NM_014714.3 P1407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:1607943 G>T maps to NM_014714.3 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr2:27676896 C>T maps to NM_015662.1 G1221G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-37-3783-01A-01D-1267-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:107938409 A>G maps to ENST00000457963 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:160102366 A>G maps to ENST00000326448 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr13:21189973 C>G maps to NM_175605.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:69353812 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:69354653 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:65621934 C>T maps to NM_004884.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr15:65623938 C>A maps to NM_004884.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:65682602 G>A maps to NM_020962.1 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:47122364 G>T maps to NM_006546.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr17:47122357 A>T maps to NM_006546.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:185407393 C>T maps to NM_006548.4 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:23391039 G>T maps to NM_006547.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:160494402 G>T maps to NM_000876.2 E1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr6:160525833 C>T maps to NM_000876.2 A2398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr6:160525908 G>T maps to NM_000876.2 S2423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr16:1842027 G>T maps to NM_001146006.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:217498632 C>T maps to NM_000597.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:46733752 C>A maps to NM_198541.1 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr19:46664045 C>A maps to NM_001002915.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:46627156 G>A maps to NM_207393.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:201195180 G>T maps to NM_001164586.1 V3572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:201193907 T>A maps to NM_001164586.1 P3464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:201195000 G>T maps to NM_001164586.1 G3512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:68696685 G>T maps to NM_002180.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr22:23237705 G>A maps to ENST00000410090 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr19:51827044 C>A maps to NM_001101372.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:130416677 G>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:130413315 C>G did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:130409716 C>G did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:130408581 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:130409703 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:130416700 G>T did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr23:130417030 C>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:130419190 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:151171200 C>T maps to NM_178822.4 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:151161029 A>T maps to NM_178822.4 L1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:151164450 G>T maps to NM_178822.4 V1106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:151161094 A>G maps to NM_178822.4 D1880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:118649068 G>T maps to NM_152538.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:118621384 C>A maps to NM_152538.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr3:118647365 G>A maps to NM_152538.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:18661418 C>T maps to NM_032880.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:18691904 G>T maps to NM_032880.4 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:18692000 C>T maps to NM_032880.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:18703337 G>T maps to NM_032880.4 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:18691940 C>T maps to NM_032880.4 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:117150579 G>T maps to NM_001542.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr1:117150570 G>T maps to NM_001542.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:41142977 C>G maps to NM_001080444.1 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:160062402 A>T maps to NM_052868.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:160061684 C>A maps to NM_052868.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:160063104 C>G maps to NM_052868.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:159901604 G>C maps to NM_001135050.1 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:159902337 G>A maps to NM_001135050.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:159900955 G>A maps to NM_001135050.1 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:159904550 T>C maps to NM_001135050.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:159900968 A>G maps to NM_001135050.1 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:133791225 G>A maps to NM_014987.1 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:133791060 G>C maps to NM_014987.1 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:219920114 G>A maps to NM_002181.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:140032729 G>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr9:111640379 T>C maps to NM_003640.3 E1250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:50467915 C>A maps to NM_006060.3 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:213886855 T>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr2:213921674 G>C maps to ENST00000342002 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:37949015 T>G maps to NM_012481.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:117860270 G>T maps to NM_001558.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:159711631 G>C did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr19:18188454 C>T maps to NM_005535.1 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:67833506 G>A did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:67816671 C>T maps to NM_001559.2 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:117900498 G>C did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:117895229 C>G did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:114238646 G>C did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:81585374 C>T maps to NM_172217.3 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr15:81598256 A>G maps to NM_172217.3 R1143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr6:52053994 G>T maps to NM_002190.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:52052552 C>G maps to NM_002190.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr16:88705513 C>T maps to NM_013278.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:52101842 C>T maps to NM_052872.3 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:17578718 C>T maps to NM_014339.5 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:17584436 C>T maps to NM_014339.5 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:9956414 C>A maps to NM_153483.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr22:50438982 G>T maps to NM_001001694.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:102988469 C>T maps to NM_003855.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:207010316 C>T maps to NM_153758.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:113537241 T>C maps to NM_000575.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:113588117 C>T maps to NM_000576.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr2:113676148 G>A maps to NM_014439.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:113670671 G>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr2:113737694 G>A maps to NM_019618.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:102781465 A>G maps to NM_000877.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr2:102632491 C>T maps to NM_004633.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr2:102626180 T>C maps to NM_004633.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr2:102644716 C>T maps to NM_004633.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:29973456 T>C did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:28807480 C>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:29973390 G>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:29301303 A>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:29972809 G>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:29973280 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:29938207 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:29972767 A>T did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:29935677 T>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:29938135 G>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:29938131 A>C did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:29973703 C>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:29959822 T>G did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:29973345 T>A did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:105011133 G>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:105011288 C>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:104984615 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:104440225 T>A did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr23:104984629 C>T did not map to a codon.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr23:104440270 C>A did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:102968089 C>T maps to NM_016232.4 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr4:123374897 G>T maps to NM_000586.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:207039696 G>A maps to NM_018724.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:137325763 T>C maps to NM_014432.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:137323264 C>T maps to NM_014432.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:136714253 A>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:123542123 G>A maps to NM_021803.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr16:27448886 C>A maps to NM_181079.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:24448053 G>A maps to NM_021258.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:24448197 C>A maps to NM_021258.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:137466873 C>A maps to NM_052962.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:56733875 C>T maps to NM_016584.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:67724261 T>C maps to NM_144701.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:68619425 T>G maps to NM_018402.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr16:28511048 G>T maps to NM_145659.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:39760577 C>T maps to NM_172138.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:6063597 G>A maps to NM_000417.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr22:37539577 A>G maps to ENST00000406505 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:70330029 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:70328192 C>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:70328446 A>C did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr16:3119199 G>T maps to ENST00000416912 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:70688510 G>A maps to NM_152456.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr23:1464293 C>T did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr16:27374478 T>A maps to NM_000418.2 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr16:27374492 C>A maps to NM_000418.2 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr16:27357842 G>T maps to NM_000418.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:27363886 A>G maps to NM_000418.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:79650856 A>T maps to NM_000880.3 L81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:35867557 C>A maps to NM_002185.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:35867467 C>T maps to NM_002185.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr5:135229764 G>A maps to NM_000590.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:135231427 C>T maps to NM_000590.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:155233217 T>C did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:155232570 G>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:155235071 G>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:155239642 C>G did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:155235766 G>C did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr3:121712683 A>T maps to ENST00000344209 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:121724178 C>T maps to ENST00000344209 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:166905974 C>A did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:166908751 T>A maps to NM_199351.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:166891993 G>A maps to NM_199351.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:153637753 C>T maps to NM_004515.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:10791696 C>T maps to NM_017620.2 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:10792703 C>T maps to NM_017620.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr19:10782045 G>A maps to NM_017620.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:110603569 T>C maps to NM_032549.2 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr8:82571594 G>A maps to NM_001144878.1 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:22007947 C>A maps to NM_018439.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr8:57905985 C>A maps to NM_017813.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:128038583 G>A maps to NM_000883.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:76712683 A>G maps to NM_001563.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:76751709 T>A maps to NM_001563.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:76715064 C>T maps to NM_001563.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:76715169 C>T maps to NM_001563.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:100949880 G>T maps to NM_016247.2 V1114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr3:100961721 C>A maps to NM_016247.2 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:100992586 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:105046811 G>A maps to NM_032727.3 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr10:105037297 G>A maps to NM_032727.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:62330262 T>G maps to NM_176877.2 Y931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr1:62293227 C>A maps to NM_176877.2 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:61919411 C>G maps to NM_001040694.1 V907V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-18-3410-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:41729529 G>A maps to NM_002192.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:57843588 A>G maps to NM_005538.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr7:30795127 G>A maps to NM_006774.4 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr7:30791873 G>A maps to NM_006774.4 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr15:41280039 G>A maps to NM_017553.1 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:33048589 C>A maps to NM_001098817.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:206911301 T>A maps to NM_017759.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:206869730 T>C maps to NM_017759.4 Q815Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr2:206921015 G>A maps to NM_017759.4 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr16:30007642 G>T maps to NM_173618.1 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:99170831 T>G maps to NM_001134224.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:99155409 C>T maps to NM_001134224.1 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr2:99185131 G>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:143003249 G>C maps to NM_003866.2 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr1:38409498 C>A maps to ENST00000373026 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr2:234102534 G>T maps to ENST00000359570 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr2:234104058 G>T maps to ENST00000359570 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:234091053 A>T did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr9:139333229 C>A maps to NM_019892.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr22:31524594 C>T maps to ENST00000331075 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr17:1416779 G>C maps to NM_016532.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr17:1399416 C>T maps to NM_016532.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:71940528 C>G maps to NM_001567.3 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr11:15197541 C>T maps to NM_001031853.3 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr11:15247262 G>A maps to NM_001031853.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr11:15260620 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:15247259 C>T maps to NM_001031853.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:155090171 G>T maps to ENST00000344756 A59A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-43-6143-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:17927796 C>A maps to NM_005543.2 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr9:5231521 G>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr14:36004315 C>A maps to NM_032594.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:7267434 C>T maps to NM_000208.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:7125331 C>A maps to NM_000208.2 E1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:7168105 C>A did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr19:7122697 G>T maps to NM_000208.2 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:7141795 C>G maps to NM_000208.2 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:156823970 G>T maps to NM_014215.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr7:1539534 G>A maps to ENST00000389470 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr7:1542594 C>T maps to ENST00000389470 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:1512807 G>A maps to ENST00000389470 F2204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr8:19677965 A>G maps to NM_018142.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr8:19687966 A>T maps to NM_018142.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr1:153735803 C>T maps to ENST00000428986 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:77705658 C>A maps to NM_033547.3 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr11:62414974 C>T maps to NM_030628.1 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:62416107 C>A maps to NM_030628.1 G482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:62416508 G>C maps to NM_030628.1 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:62415254 G>T maps to NM_030628.1 S766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:62417263 A>T maps to NM_030628.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:212180085 C>T maps to NM_015434.3 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:212151613 C>A maps to NM_015434.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:95848774 A>T maps to NM_017864.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:95888701 T>C maps to NM_017864.2 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr8:28695254 G>T maps to NM_018250.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr4:128584729 A>G maps to NM_015693.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr4:128584543 G>T maps to NM_015693.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:59986885 G>A maps to NM_152230.4 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:61802097 C>T maps to NM_001134779.1 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:44424464 C>T maps to NM_014652.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:44422279 C>A maps to NM_014652.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:24656299 G>A maps to ENST00000458132 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:30806003 G>A maps to NM_006390.3 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:30805223 C>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:201839745 G>A maps to NM_018085.4 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:46211818 G>A maps to NM_005897.2 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:46180007 C>A maps to NM_005897.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr9:95411766 C>A maps to NM_022755.5 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:237272467 G>T maps to ENST00000457693 Y616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr2:237240049 C>T maps to ENST00000457693 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr2:237246992 G>A maps to ENST00000457693 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:237405853 C>A maps to ENST00000457693 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:121508985 G>A maps to NM_001023570.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr3:51895935 A>C maps to NM_203424.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr3:51864597 G>T maps to NM_001085479.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr15:67681238 A>G maps to NM_001031715.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:158980334 A>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:158983041 C>A maps to NM_001042705.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:158980416 C>G maps to NM_001197113.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr16:19741815 G>T maps to NM_153208.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:91037998 G>T maps to NM_003870.3 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr15:90999475 G>T maps to NM_003870.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr15:91027568 C>T maps to NM_003870.3 I1302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr5:75950039 C>T maps to NM_006633.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr5:75950760 T>C maps to NM_006633.2 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:156526477 G>A maps to NM_178229.4 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:156499986 C>A maps to NM_178229.4 R1438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:156513992 C>T maps to NM_178229.4 W804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:156503908 C>T maps to NM_178229.4 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr23:53279722 G>A did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:53279920 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:53277928 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:53284069 C>T did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:247965 G>C maps to NM_001170738.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:248088 A>T maps to NM_001170738.1 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:247986 G>T maps to NM_001170738.1 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:123119902 T>C maps to NM_178827.4 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:123104991 T>C maps to NM_178827.4 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr7:123109369 G>A maps to NM_178827.4 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr7:123092883 A>T maps to NM_178827.4 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:153284160 G>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:153279679 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:153279560 G>C did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:153279713 C>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:153278531 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:10268099 C>T maps to NM_001570.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:10283899 C>G maps to NM_001570.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:66620556 G>A maps to NM_007199.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:66605325 A>T maps to NM_007199.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:78755399 C>T maps to NM_004136.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr15:78783001 T>C maps to NM_004136.2 H741H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr15:78764102 G>A maps to NM_004136.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr15:78782998 C>G maps to NM_004136.2 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr4:185320123 C>T maps to NM_002199.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr6:401481 G>A maps to NM_002460.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr7:128587849 C>G maps to NM_001098629.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:209969719 G>A maps to NM_006147.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:209965772 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:209964184 G>A maps to NM_006147.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr11:612716 G>A maps to NM_004031.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr14:24633865 G>A maps to NM_006084.4 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:44222961 G>A maps to NM_019612.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:44223960 G>C maps to NM_019612.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:44223250 C>A maps to NM_019612.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:44223576 C>A maps to NM_019612.3 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:44223366 G>T maps to NM_019612.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:227662073 C>A maps to NM_005544.2 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:227663166 C>A maps to NM_005544.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:110434647 G>C maps to NM_003749.2 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr23:107977057 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:107975872 G>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:107976319 T>C did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:107977074 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:107978979 G>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:107979217 C>A did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:107977873 C>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:107979493 T>A did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:3599449 C>A maps to NM_024337.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr16:54967520 G>A maps to NM_005853.5 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:55361549 G>T maps to NM_024335.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:108960977 T>C maps to NM_213595.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:50683494 A>T maps to NM_002202.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr5:50680534 G>A maps to NM_002202.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:76633488 G>A maps to NM_145805.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr15:74468266 G>A maps to NM_201526.1 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:74467561 C>T maps to NM_201526.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:74425283 C>T maps to NM_001130137.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:74425430 C>T maps to NM_001130137.1 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:74425601 G>T maps to NM_001130137.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:74425688 C>T maps to NM_001130137.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:74425917 C>T maps to NM_001130137.1 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr14:77944916 C>G did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr14:77948968 C>T maps to NM_199296.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:128440725 C>T maps to NM_016048.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:128442720 C>G maps to NM_016048.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr22:35478544 C>T maps to NM_001008494.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr22:35478550 C>A maps to NM_001008494.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:128875485 C>T maps to ENST00000418265 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:128852993 G>T maps to ENST00000418265 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr16:47196507 C>T maps to NM_030790.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:2929369 G>A maps to NM_018463.3 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:2930909 A>C maps to NM_018463.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr16:312510 G>A maps to NM_032039.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:52223412 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:52235522 T>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:145536082 G>C maps to NM_003637.3 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:145537198 C>T maps to NM_003637.3 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:68617467 C>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr15:68618990 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr15:68603376 G>A maps to ENST00000423218 Y1044Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr15:68624759 C>A maps to ENST00000423218 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr15:68631961 G>A maps to ENST00000423218 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:52374694 C>T maps to NM_002203.3 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:48145586 G>T maps to NM_002204.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr12:54794635 G>A maps to NM_002205.2 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:54795379 G>A maps to NM_002205.2 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr2:173349563 C>G maps to ENST00000264106 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:173362746 G>A maps to ENST00000264106 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr2:173356151 G>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr12:56078922 G>A maps to ENST00000347027 G1155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:56079051 C>T maps to ENST00000347027 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr12:56094857 C>T maps to ENST00000347027 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr12:56086981 G>A maps to ENST00000347027 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr10:15600084 A>C maps to NM_003638.1 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:15573046 A>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:15702877 A>G maps to NM_003638.1 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr10:15614301 G>T maps to NM_003638.1 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr10:15686209 G>T maps to NM_003638.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr10:15600081 T>C maps to NM_003638.1 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr10:15688890 A>G maps to NM_003638.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:37778402 C>T maps to NM_002207.2 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:31425841 C>T maps to ENST00000444228 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr16:31419089 G>T maps to ENST00000444228 G304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:31425869 C>A maps to ENST00000444228 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr16:31424156 A>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:31435469 C>T maps to ENST00000444228 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:31419187 C>T maps to ENST00000444228 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr17:3704417 C>A maps to NM_002208.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr16:30522394 G>T maps to NM_002209.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr16:31332937 G>T maps to NM_001145808.1 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr16:31341847 C>A maps to NM_001145808.1 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:187455139 A>G maps to NM_002210.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:187523841 T>A maps to NM_002210.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:31374071 C>T maps to NM_000887.3 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr16:31382732 G>A maps to NM_000887.3 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr16:31391089 G>T maps to NM_000887.3 G961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr16:31391845 A>C maps to NM_000887.3 I1059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:33200847 G>A maps to ENST00000374956 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr2:9558756 T>A maps to NM_004763.3 K24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:70524053 C>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:70524910 C>G did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:70524082 T>C did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr21:46330675 G>A maps to NM_000211.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr21:46310004 C>A maps to NM_000211.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr17:45368429 T>C maps to NM_000212.2 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:63920138 C>T maps to ENST00000371092 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr17:73732370 C>T maps to NM_001005619.1 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:73747074 C>T maps to NM_001005619.1 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr17:73732130 G>A did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:53585732 C>A maps to NM_000889.1 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:53590368 G>T maps to NM_000889.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr7:20418788 C>T maps to NM_002214.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:52818336 C>A maps to NM_002215.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr10:7759669 C>T maps to NM_002216.2 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:7762922 G>A maps to NM_002216.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:52852088 G>A maps to ENST00000485816 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr10:7659225 T>A maps to ENST00000256861 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:7608014 G>T maps to ENST00000256861 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:7679441 C>G did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr10:7679269 G>T maps to ENST00000256861 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:7618474 G>T maps to ENST00000256861 S640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr10:7683936 C>T maps to ENST00000256861 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:54786270 C>T did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:54800575 C>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:54783782 G>T did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:54783730 G>T did not map to a codon.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr23:54814965 C>G did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:54776339 G>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:54784646 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:54784060 G>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:54785032 C>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:54780107 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:54823399 G>C did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:54784797 C>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:54783661 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:54776514 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:54783526 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:54784426 G>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:54814947 C>T did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr5:156638379 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:156608050 T>A maps to NM_005546.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:160850480 A>T maps to NM_017625.2 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:160920952 C>A maps to NM_080878.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:160917717 C>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:78619024 T>C did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:78618611 A>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:78622692 T>C did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:78618571 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:93483147 T>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:226827341 C>T maps to NM_002221.3 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:226924190 G>A maps to NM_002221.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:226924301 C>G maps to NM_002221.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:226924703 C>T maps to NM_002221.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:226923322 C>A maps to NM_002221.3 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:41231344 G>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:41235272 G>T maps to NM_025194.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr3:4725141 G>T maps to ENST00000356617 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:4683775 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:26868708 G>A maps to NM_002223.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:26572032 G>A maps to NM_002223.2 V2353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr12:26775338 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:26807025 C>A maps to NM_002223.2 G875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:26636759 G>T maps to NM_002223.2 C1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr12:26709221 T>C maps to NM_002223.2 E1636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:33641417 C>G maps to ENST00000374316 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:33638468 G>T maps to ENST00000374316 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:106075071 G>A maps to NM_033397.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:106074525 G>A maps to NM_033397.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:96993223 G>C maps to ENST00000420728 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:96993430 G>T maps to ENST00000420728 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:96992836 C>A maps to ENST00000420728 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr21:35127599 A>T did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr21:35144462 G>T maps to NM_003024.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr21:35140085 A>G maps to NM_003024.2 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:24435596 C>A maps to NM_006277.2 R1337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:24435599 C>A maps to NM_006277.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:24524940 C>T maps to NM_006277.2 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:24427168 G>C maps to NM_006277.2 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:24494809 C>T maps to NM_006277.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr15:40702941 C>T maps to NM_002225.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr15:40705251 C>A maps to NM_002225.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:185270620 A>C maps to NM_006469.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:185270567 G>C maps to NM_006469.4 S298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:128262760 C>A maps to NM_017969.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:128281367 C>G did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr20:10622442 G>A maps to NM_000214.2 I890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr20:10639145 C>A maps to NM_000214.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr20:10621760 A>T maps to NM_000214.2 I1016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:65310569 C>T maps to NM_002227.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:65339168 C>A maps to NM_002227.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:5078316 C>T maps to NM_004972.3 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr9:5070052 G>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr19:17950439 G>A maps to NM_000215.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:6043915 G>A maps to NM_001099433.1 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr4:6107433 C>G maps to NM_001099433.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr4:6083356 G>T maps to NM_001099433.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:147040804 G>A maps to NM_014790.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr5:147029987 C>A maps to NM_014790.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr10:133967421 G>T maps to NM_001105521.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:133930771 G>A maps to NM_001105521.2 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr10:133978214 A>G maps to NM_001105521.2 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:134014176 C>T maps to NM_032801.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:15496634 C>T maps to NM_004973.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr6:15507458 A>C maps to NM_004973.2 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:15511633 T>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr6:15496844 G>T maps to NM_004973.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr7:27934860 T>C maps to NM_175061.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:64943276 T>C maps to NM_032776.1 E2338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:27221542 G>C maps to NM_001145348.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:74717908 C>A maps to NM_001081461.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:42139650 C>T maps to NM_005090.3 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr22:39085043 G>C maps to NM_014876.5 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr19:51013559 G>A maps to NM_138334.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:75227316 C>T maps to NM_020647.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr20:42744724 C>A maps to NM_020433.4 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr16:87723730 C>A maps to NM_020655.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr14:24040343 G>T maps to NM_032452.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:96125202 G>T maps to NM_003772.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr14:23444074 G>A maps to NM_032876.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:59248538 C>A maps to NM_002228.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr19:12903532 C>G maps to NM_002229.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr17:39913762 G>A maps to NM_021991.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr6:24358064 G>A maps to NM_181337.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:8503660 T>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:8501093 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:124201666 C>A maps to NM_001024660.3 R1400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:124385399 C>T maps to NM_001024660.3 L2149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr3:124209607 G>T maps to NM_001024660.3 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr3:124132411 G>A maps to NM_001024660.3 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:124431835 G>T maps to NM_001024660.3 V2710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:124281800 G>T maps to NM_001024660.3 E1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr3:124380706 G>T maps to NM_001024660.3 E2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr3:124153218 C>T maps to NM_001024660.3 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr19:8389684 G>A maps to NM_198471.2 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:62739161 G>T maps to NM_181712.4 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:62740490 C>A maps to NM_181712.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:62739200 G>T maps to NM_181712.4 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:20189782 C>T maps to NM_003884.4 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:65480519 G>A maps to NM_182710.1 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:149919435 G>A maps to NM_007044.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr18:44595925 C>A maps to ENST00000356157 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr18:44586019 C>T maps to ENST00000356157 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr16:57778364 C>G maps to NM_005886.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:15428225 C>T maps to NM_201628.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:170366614 G>A maps to NM_006063.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:127646666 C>A maps to NM_207335.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:105923773 C>A maps to NM_198439.2 G548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:105924320 T>C maps to NM_198439.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr3:42728189 G>A maps to NM_152393.2 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:42730525 G>T maps to NM_152393.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:42728048 C>G maps to NM_152393.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr3:42727964 G>A maps to NM_152393.2 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr13:41704623 C>T maps to NM_152903.4 *675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr13:41767239 G>T maps to NM_032138.4 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr12:5021035 G>T maps to NM_000217.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr1:111060833 C>T maps to NM_005549.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:111147296 C>G maps to NM_004974.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:30032974 G>A maps to NM_002233.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:30033958 C>A maps to NM_002233.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:30032758 G>T maps to NM_002233.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:30033379 C>T maps to NM_002233.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:30033007 G>A maps to NM_002233.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:30034012 A>T maps to NM_002233.2 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:5153900 C>T maps to NM_002234.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:5153870 G>A maps to NM_002234.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:4920787 G>T maps to NM_002235.3 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:4920412 C>T maps to NM_002235.3 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:4919971 G>T maps to NM_002235.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr19:49575578 G>A maps to NM_031886.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr3:156232995 C>A maps to NM_172159.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:156254472 G>T maps to NM_172159.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:75444794 C>A maps to NM_139137.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr12:75444821 C>A maps to NM_139137.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:110754585 G>A maps to NM_004978.4 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:110754720 C>A maps to NM_004978.4 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:110765933 C>T maps to NM_004978.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:48825895 C>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:48825920 G>T did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:48826209 C>T did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr7:119914820 G>C maps to NM_012281.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr7:119915249 C>T maps to NM_012281.2 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:112525140 C>A maps to ENST00000315987 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:11053970 C>T maps to NM_002236.4 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:11053749 C>T maps to NM_002236.4 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr20:49626383 G>A maps to NM_002237.3 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr18:77659302 C>G maps to NM_012283.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr16:84270968 G>T maps to NM_172347.2 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:84271025 A>G maps to NM_172347.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:84270758 G>A maps to NM_172347.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr16:84270968 G>T maps to NM_172347.2 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:211093060 G>A maps to NM_172362.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:211192445 A>T maps to NM_172362.2 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:211093084 C>A maps to NM_172362.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:211256145 G>T maps to NM_172362.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:211192562 G>C maps to NM_172362.2 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:210856670 C>A maps to NM_172362.2 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:150644066 G>A maps to NM_000238.2 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:49933229 C>T maps to NM_012284.1 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr12:49951430 C>T maps to NM_012284.1 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr12:49936561 G>T maps to NM_012284.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr12:49948270 G>T maps to NM_012284.1 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:40317580 C>T maps to NM_012285.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:63269104 G>A maps to NM_139318.3 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr14:63447642 G>A maps to NM_139318.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr14:63174852 A>G maps to NM_139318.3 D780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr14:63174750 G>C maps to NM_139318.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr17:61615850 T>C maps to NM_030779.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:163291735 G>A maps to NM_033272.2 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr2:163393570 G>A maps to NM_033272.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:163693137 G>A maps to NM_033272.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:163374450 G>T maps to NM_033272.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:163302602 G>A maps to NM_033272.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:163693136 C>A maps to NM_033272.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr3:19295335 G>A maps to NM_144633.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:19436803 G>A did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr3:19295284 G>T maps to NM_144633.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:96040089 A>G maps to NM_013434.4 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:21699021 C>T maps to NM_001035003.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:20751283 C>T did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr4:20852180 G>C maps to ENST00000382152 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:160012155 C>T maps to NM_002241.4 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr17:21319283 C>T maps to NM_021012.4 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:21319496 C>T maps to NM_021012.4 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr17:21319682 G>A maps to NM_021012.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr21:39672220 T>C maps to NM_170736.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:39671704 G>C maps to NM_170736.1 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr17:68129005 G>T maps to NM_018658.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr17:68171776 C>T maps to NM_000891.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr17:68171452 T>G maps to NM_000891.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:128781485 C>T maps to NM_000890.3 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr11:128781410 G>T maps to NM_000890.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr11:128786379 C>T maps to NM_000890.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr21:39087404 G>A maps to NM_002240.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr21:39086790 C>G maps to NM_002240.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:21926475 C>G maps to NM_004982.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:21919016 G>A maps to NM_004982.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:21919229 A>G maps to NM_004982.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:160054284 C>A maps to NM_004983.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr14:88707110 G>A maps to NM_138318.2 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:88651980 C>T maps to NM_138318.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr14:88654342 G>A maps to NM_138318.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:47748347 G>T maps to NM_022055.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr14:90650581 C>A maps to NM_022054.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:39285660 G>T maps to NM_032115.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:39290232 A>G maps to NM_032115.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:39271837 G>A maps to NM_031460.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:39271745 G>T maps to NM_031460.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr10:118969567 G>T maps to NM_181840.1 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:215408272 C>T maps to NM_001017425.2 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:26951213 G>A maps to NM_002246.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:64064612 C>A maps to ENST00000422670 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:39162005 G>T maps to NM_003740.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:65360631 G>A maps to NM_033347.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr8:140630668 G>A maps to NM_016601.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr8:140630899 G>A maps to NM_016601.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:140630638 G>T maps to NM_016601.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr8:140631067 G>A maps to NM_016601.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr8:140631211 G>C maps to NM_016601.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr10:79011014 C>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:78880777 C>T maps to NM_001161352.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:78943264 C>T maps to NM_001161352.1 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr5:169810699 G>T maps to NM_004137.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:178560679 G>A maps to NM_005832.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:70824331 C>T maps to NM_014505.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr5:113831626 A>G maps to NM_021614.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:113831665 C>A maps to NM_021614.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:154841807 G>A maps to NM_002249.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:2604669 A>T maps to NM_000218.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:62065175 G>C maps to NM_172107.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr20:62076080 C>T maps to NM_172107.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr20:62038506 C>T maps to NM_172107.2 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr20:62065178 G>T maps to NM_172107.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr20:62076600 G>A maps to NM_172107.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:133142110 C>A maps to NM_004519.2 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr8:133153496 C>A maps to NM_004519.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:133150166 G>T maps to NM_004519.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:41283879 G>A maps to NM_004700.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:73713678 C>T maps to NM_001160133.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:73713721 G>C did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr13:50590024 A>G maps to NM_173605.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:43723775 G>T maps to NM_002251.3 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr20:43723627 G>A maps to NM_002251.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:99440425 C>A maps to NM_020697.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:18113461 T>A maps to NM_002252.3 L396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr9:138669263 C>A maps to ENST00000298480 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:196227411 C>T maps to NM_198503.2 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:196461393 G>C maps to NM_198503.2 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:196311206 A>C did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:196342286 A>G maps to NM_198503.2 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:196205138 G>A maps to NM_198503.2 T1091T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:196436901 G>A maps to NM_198503.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:36673127 C>T maps to NM_001031836.2 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:36703340 C>T maps to NM_001031836.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:36698063 T>C maps to NM_001031836.2 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:110980598 G>A maps to NM_014379.2 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:110984529 C>G maps to NM_014379.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr8:110986305 G>A maps to NM_014379.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr9:2718959 C>A maps to NM_133497.2 C407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr9:2718878 C>A maps to NM_133497.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr12:109895803 G>T maps to NM_031954.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:7256758 C>T maps to NM_001002914.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:77727788 C>G maps to NM_023930.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:77727701 C>T maps to NM_023930.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr16:67327990 G>T maps to NM_001100915.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:77885470 G>A maps to NM_001029859.1 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:215777493 G>T maps to NM_016121.3 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:215793753 G>T maps to NM_016121.3 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:2749841 C>T maps to NM_018992.3 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr7:66103966 C>G maps to NM_153033.3 L206L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-18-5592-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr4:44177019 T>G maps to NM_198353.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:44449796 G>A maps to NM_198353.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr4:44177250 T>A maps to NM_198353.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr4:44449870 G>A maps to NM_198353.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:25315738 C>T maps to NM_017634.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr13:103440246 T>C maps to NM_024089.2 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:23395629 G>T maps to NM_001009999.2 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr12:121958789 G>T maps to ENST00000377071 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:121958889 G>A maps to ENST00000377071 A315A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-66-2754-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:86705770 G>A maps to NM_001146688.1 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr2:86711187 G>T maps to NM_001146688.1 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:86719208 G>A maps to NM_001146688.1 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr2:86693608 G>A maps to NM_001146688.1 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr5:137727931 C>A maps to NM_016604.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr5:137721892 A>G maps to NM_016604.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:44126005 G>T maps to NM_014663.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:5077468 C>T maps to NM_015015.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr19:5133936 C>T maps to NM_015015.2 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:7174611 G>T maps to NM_015061.3 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr9:6984309 G>A maps to NM_015061.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr9:7013901 G>T maps to NM_015061.3 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:94731243 G>C maps to NM_018039.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr11:94731333 G>A maps to NM_018039.2 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr11:94731717 G>C maps to NM_018039.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:94731216 C>A maps to NM_018039.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:475234 G>T maps to NM_001042603.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr12:401957 T>G maps to NM_001042603.1 A1611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:464403 G>A maps to NM_001042603.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:427393 C>G maps to NM_001042603.1 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr12:475138 G>C maps to NM_001042603.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:53250046 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:53228047 G>T did not map to a codon.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr23:53241054 C>G did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr23:53230855 T>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:53246996 T>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:53231061 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr24:21868706 C>A did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr24:21901520 C>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr24:21894628 C>A did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr24:21868201 C>G did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:44922693 C>T did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:44896928 A>G did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:44970625 G>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr23:44937642 A>G did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:44941829 G>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:44936071 G>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:44929601 G>A did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:7751546 C>T maps to NM_001080424.1 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:55970834 G>T maps to NM_002253.2 C654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:55979623 G>A maps to NM_002253.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:55961109 G>T maps to NM_002253.2 R944R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:55974022 A>T maps to NM_002253.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr4:55955888 A>G maps to NM_002253.2 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr4:55972047 C>A maps to NM_002253.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr4:55953822 C>A maps to NM_002253.2 E1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr19:10610486 G>A maps to NM_203500.1 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:142638488 C>T maps to NM_000420.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:91449569 G>A maps to NM_007035.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr6:62604626 A>G maps to NM_152688.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:62407150 C>A maps to NM_152688.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:136619235 G>A maps to NM_006558.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr14:24900890 C>T maps to NM_015299.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr19:6420433 C>A maps to NM_003685.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr17:26967584 G>A maps to NM_014680.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr17:26967594 G>C maps to NM_014680.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr17:26964039 T>C maps to NM_014680.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:48614342 G>T maps to NM_001080394.1 G612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:48647945 G>A maps to NM_001080394.1 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:73492461 C>T maps to ENST00000375248 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr17:73486808 C>T maps to ENST00000375248 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr17:73489112 C>G maps to ENST00000375248 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr17:73494305 C>A maps to ENST00000375248 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr17:73487780 C>A maps to ENST00000375248 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:126071655 G>A maps to ENST00000377985 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:126079899 C>T maps to ENST00000377985 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:197431509 G>T maps to NM_014687.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:197410252 C>T maps to NM_014687.1 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr6:42823595 G>T maps to NM_015349.1 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr14:105344819 C>T maps to ENST00000453495 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:75134183 C>A maps to NM_001039479.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:35909834 C>A maps to NM_024874.4 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:35921738 G>A maps to NM_024874.4 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr19:34791500 G>C maps to NM_014686.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:34833289 C>A maps to NM_014686.3 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:34818702 G>T maps to NM_014686.3 G292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr9:114176210 C>T maps to NM_001080398.1 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:114182344 G>C maps to NM_001080398.1 S682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr9:114246756 A>C maps to NM_001080398.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:35592856 G>T maps to NM_014672.2 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr20:36625154 G>A maps to NM_014657.1 D998D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr20:36641555 G>A maps to NM_014657.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr20:36640670 C>G maps to NM_014657.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr7:4823973 C>G maps to ENST00000450194 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr7:4815353 C>A maps to ENST00000450194 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr18:46145965 C>T maps to NM_001142397.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr16:15690594 G>C maps to NM_014647.3 V1728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:43898204 C>T maps to NM_015284.2 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:43897157 G>T maps to NM_015284.2 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:43915781 G>A maps to NM_015284.2 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:47154047 T>A maps to NM_014774.2 K322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr16:85100944 G>T maps to NM_014732.2 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr16:85111095 A>T maps to NM_014732.2 K214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr12:22637740 G>A maps to ENST00000446597 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr12:22635540 C>A maps to ENST00000446597 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr12:22676468 C>A maps to ENST00000446597 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr16:27772788 T>G maps to NM_015202.2 T1229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:3761502 G>A maps to NM_014704.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr14:58915140 C>T maps to ENST00000354386 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr14:58896151 G>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr11:46690952 G>C did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:55356571 C>T maps to NM_001098815.1 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr17:6483096 G>A maps to NM_014804.2 F958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr17:6531661 C>A maps to NM_014804.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr17:6499543 G>T maps to NM_014804.2 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:39878641 C>G maps to NM_015038.1 S902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:96984165 G>T maps to NM_015323.4 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr6:97001373 G>T maps to NM_015323.4 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr18:8783854 G>T maps to ENST00000456698 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr18:8825137 T>C maps to ENST00000456698 G1529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr18:8798271 G>T maps to ENST00000456698 G1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr14:55878323 C>A maps to NM_014924.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr14:55878362 G>A maps to NM_014924.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr14:55848688 G>A maps to NM_014924.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr7:36373698 C>A maps to NM_001100425.1 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:75557616 C>T maps to NM_015037.2 F1247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:75549947 C>G maps to NM_015037.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:75550014 G>T maps to NM_015037.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr10:75558774 G>T maps to NM_015037.2 E1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr4:154525133 C>A maps to NM_001131007.1 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:154557705 C>A maps to NM_001131007.1 S1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr4:154502647 C>T maps to NM_001131007.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:154548807 T>A maps to NM_001131007.1 P1392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr5:5463103 C>A maps to NM_015325.1 Y1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:5463892 G>A maps to NM_015325.1 E1482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr5:5489358 G>T maps to NM_015325.1 R2239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:5462756 G>T maps to NM_015325.1 G1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr5:5463178 G>T maps to NM_015325.1 S1244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr5:5465332 A>C maps to NM_015325.1 T1962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:5462572 A>G maps to NM_015325.1 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr5:5461157 G>T maps to NM_015325.1 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr5:5464054 G>A maps to NM_015325.1 A1536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:84884583 C>G maps to NM_014895.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr18:29493399 G>A maps to NM_014939.3 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr15:79750081 T>C maps to NM_015206.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr15:79755578 G>A maps to NM_015206.2 V823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:79750589 A>T maps to NM_015206.2 K701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr15:79749055 C>G maps to NM_015206.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:79760689 C>A maps to NM_015206.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr4:123160880 T>C maps to NM_015312.3 S1348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:123245613 T>C maps to NM_015312.3 S3609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:123260372 C>T maps to NM_015312.3 I4054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:123260426 C>A maps to NM_015312.3 S4072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr4:123161456 C>A maps to NM_015312.3 T1540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr4:123107279 G>T maps to NM_015312.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr4:123283400 A>G maps to NM_015312.3 *5006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr4:123270433 G>T maps to NM_015312.3 G4468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr4:123268788 C>T maps to NM_015312.3 S4328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:123175390 T>C maps to NM_015312.3 P1988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr9:34372104 C>G maps to NM_020702.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr9:34371051 A>C maps to NM_020702.3 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:81212547 C>A maps to NM_018689.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr15:81181911 C>T maps to NM_018689.1 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr23:118215437 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:118221160 T>C did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:118220626 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:118215377 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:118242298 C>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:118230555 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:118223501 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:118243103 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:118220997 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:118222334 G>T did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:118230626 C>G did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:118222606 A>C did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:118222756 T>C did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr4:57190271 C>A maps to NM_020722.1 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:57181914 C>A maps to NM_020722.1 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr10:24790395 C>A maps to NM_019590.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:24813692 G>A maps to NM_019590.3 E966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr10:24783455 G>A maps to NM_019590.3 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr10:24833112 G>A maps to NM_019590.3 V1638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr6:138607836 G>C did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:138655784 C>T maps to NM_020340.4 G1934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:138531057 G>A maps to NM_020340.4 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr6:138655302 C>T maps to NM_020340.4 L1774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:44248239 C>A maps to NM_015443.3 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr17:44249080 C>A maps to NM_015443.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:44109490 A>G maps to NM_015443.3 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr17:44110444 C>G did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr10:72289797 C>T maps to NM_014431.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:86539299 G>A maps to NM_001142749.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr15:52902291 C>T maps to NM_019600.2 W273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:101834489 C>T maps to NM_020802.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:101834522 G>A maps to NM_020802.2 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:232942721 G>T maps to NM_019090.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:232941914 A>G maps to NM_019090.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:113755616 C>T maps to NM_020817.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr3:113721325 T>A maps to NM_020817.1 K680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:94044261 T>C maps to ENST00000393153 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr14:94008942 G>A maps to ENST00000393153 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr14:94088543 C>T maps to ENST00000393153 G1677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr14:94067099 A>G maps to ENST00000393153 E1186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:94084611 G>T maps to ENST00000393153 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:94158225 G>A maps to ENST00000393153 L2529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:94079209 C>T maps to ENST00000393153 H1296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr14:94088265 G>T maps to ENST00000393153 E1585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr14:94053011 C>T maps to ENST00000393153 T958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:95539318 A>G maps to NM_015496.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr8:95511669 T>A maps to NM_015496.3 K1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:95501055 T>G maps to NM_015496.3 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr8:95507086 C>G did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr8:95543305 C>A maps to NM_015496.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:5763162 A>G maps to ENST00000414202 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr9:5763760 C>T maps to ENST00000414202 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr9:5765671 C>G maps to ENST00000414202 S1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:30315230 C>T maps to NM_020848.2 Q1282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr10:30316391 C>T maps to NM_020848.2 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:30318359 C>T maps to NM_020848.2 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr10:30317315 C>T maps to NM_020848.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:30317687 C>G maps to NM_020848.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:30318353 C>T maps to NM_020848.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr10:30315899 C>T maps to NM_020848.2 Q1059Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr10:30316849 G>A maps to NM_020848.2 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr2:226447575 G>C maps to NM_020864.1 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:226446957 C>T maps to NM_020864.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:226273725 C>A maps to NM_020864.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:108300320 C>A maps to NM_020890.2 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr3:108276189 C>A maps to NM_020890.2 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr9:100139101 C>T maps to ENST00000375206 Q1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr4:1379709 C>T maps to NM_020894.2 H697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr9:35105946 G>T maps to NM_025182.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr9:35107388 C>A maps to NM_025182.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr19:7676773 C>A maps to NM_001080429.2 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:7682717 G>A maps to NM_001080429.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:138554435 G>A maps to NM_001164665.1 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:138554321 C>A maps to NM_001164665.1 T1579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr7:138522833 C>T maps to NM_001164665.1 E1890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:138566134 T>G maps to NM_001164665.1 R1410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:138591709 C>A maps to NM_001164665.1 E1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr7:138601662 G>A maps to NM_001164665.1 D903D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:138603933 C>A maps to NM_001164665.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:180886162 C>A maps to NM_020950.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr18:43532398 G>A maps to NM_020964.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr18:43456278 C>A maps to NM_020964.2 E1991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr18:43446903 C>A maps to NM_020964.2 S2160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr18:43531082 G>C maps to NM_020964.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr18:43438726 C>A maps to NM_020964.2 G2344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr18:43519603 C>A maps to NM_020964.2 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr22:44696780 G>A maps to NM_001099294.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr19:18368564 G>T maps to NM_001145304.1 R1177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:176812319 T>C maps to NM_030650.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:176794703 C>T maps to NM_030650.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:176829139 C>T maps to NM_030650.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr14:77579781 C>G maps to NM_033426.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:1897927 A>T maps to ENST00000434971 L428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr20:36854087 G>T maps to NM_001029864.1 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr20:36841983 C>G maps to NM_001029864.1 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr9:20862692 C>A maps to NM_017794.3 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:20764906 G>T maps to NM_017794.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:233482293 A>T maps to NM_032435.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr11:105880330 C>T maps to NM_032424.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:30653371 C>A maps to NM_133471.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr9:115421862 C>G maps to NM_133465.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr9:115337068 A>T maps to NM_133465.2 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:22472970 G>T maps to NM_021174.5 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr9:139693671 G>A maps to NM_001039374.4 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:11983448 C>T maps to ENST00000376576 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr3:113378935 T>C maps to NM_001009899.2 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:73963357 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:73961212 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:73962754 T>A did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:73963357 C>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:73963888 C>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:73960440 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:73960134 G>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:73963302 T>C did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr23:73959295 A>T did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:73963348 C>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:73963707 C>A did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr23:73960685 T>C did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr9:5921510 C>T maps to NM_001017969.2 A1495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr9:5988343 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:8890322 G>A maps to NM_020738.2 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr2:8871134 G>A maps to NM_020738.2 N1677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr2:8952523 C>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr2:8938352 A>C maps to NM_020738.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr10:94409661 C>G maps to NM_004523.3 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr9:116857502 G>T maps to ENST00000259410 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr9:116854705 G>T maps to ENST00000259410 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:17809079 G>A maps to NM_022113.4 F694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr6:17781125 T>A maps to NM_022113.4 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:17764628 G>A maps to NM_022113.4 S1710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr8:29003963 C>T maps to NM_015254.3 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:200567387 C>A maps to NM_014875.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:44893440 C>A maps to NM_020242.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:44839158 C>T maps to NM_020242.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr20:16336977 G>A maps to NM_024704.4 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr20:16359630 C>A maps to NM_024704.4 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr20:16362392 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:21014321 C>T maps to NM_020816.2 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:20991136 G>A maps to NM_020816.2 I1010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:21031087 C>T maps to NM_020816.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:21031123 C>T maps to NM_020816.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:21031279 G>C maps to NM_020816.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:21036132 C>T maps to NM_020816.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:21042066 G>A maps to NM_020816.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr11:28058071 A>G maps to NM_031217.3 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr11:28058211 C>A did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr17:43013654 G>T maps to ENST00000438933 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr17:43004446 C>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr17:43012641 G>C maps to ENST00000438933 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr17:72344019 C>A maps to NM_153209.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:72346633 G>T maps to NM_153209.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:241689957 G>A maps to ENST00000373308 F955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:241685276 C>A maps to ENST00000373308 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:241658611 C>A maps to ENST00000373308 P1683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:10384042 C>T maps to ENST00000377086 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:10336421 G>T maps to ENST00000377086 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:10425164 G>A maps to ENST00000377086 Q1458Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:10386246 C>T maps to ENST00000377086 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:137520076 C>G maps to NM_005733.2 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr10:91486249 C>A maps to ENST00000416354 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:91497624 C>G maps to ENST00000416354 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr10:91533729 T>A maps to ENST00000416354 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:39734804 C>A maps to ENST00000395670 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr12:39751146 A>T maps to ENST00000395670 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr12:39763665 G>A maps to ENST00000395670 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:39716582 G>T maps to ENST00000395670 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:39751146 A>T maps to ENST00000395670 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:200959777 G>A maps to NM_017596.2 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:200955981 G>A maps to NM_017596.2 Q1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr15:69709735 G>A maps to NM_138555.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:168443316 C>T maps to NM_030615.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:168430289 C>T maps to NM_030615.2 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr14:104641908 C>T maps to NM_015656.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr14:104643060 G>T maps to NM_015656.1 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr14:104638964 G>T maps to NM_015656.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:86468573 A>G maps to NM_017576.1 I1109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr17:51901107 C>A maps to NM_032559.4 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr17:51902220 C>A maps to NM_032559.4 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr17:51901476 G>A maps to NM_032559.4 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:51900534 G>T maps to NM_032559.4 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:51901692 G>T maps to NM_032559.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:51901866 C>T maps to NM_032559.4 H491H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:51901584 G>T maps to NM_032559.4 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:45232772 C>T maps to NM_006845.3 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:30898383 C>A maps to NM_004798.3 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:69626793 G>T did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:69595964 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:69561720 A>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:69615552 C>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:69510563 C>G did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:69561757 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:154394591 G>A maps to NM_001099293.1 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:154393631 G>T maps to NM_001099293.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:57957890 G>T maps to NM_004984.2 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:57966466 G>T maps to NM_004984.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr12:57969022 G>T maps to NM_004984.2 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr10:32306104 C>T maps to NM_004521.2 K909K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr10:32322781 A>C maps to NM_004521.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:149840132 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:149806961 G>C maps to NM_004522.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:149840147 C>A maps to NM_004522.1 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr2:149838056 C>T maps to NM_004522.1 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr15:90171693 G>A maps to NM_198525.2 R1330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr3:47316964 A>G maps to NM_182902.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:169985705 C>T maps to NM_014970.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:169951128 G>A maps to NM_014970.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:145693753 G>T maps to NM_145754.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:145698043 C>T maps to NM_145754.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr8:145692605 G>T maps to NM_145754.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:7829788 C>T maps to NM_012311.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:55285041 C>T maps to ENST00000291633 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:55263134 C>G maps to NM_015868.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:55316353 G>C maps to ENST00000396289 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:55349151 G>A maps to NM_012314.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:55351039 G>A maps to NM_012314.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:55349310 T>C maps to NM_012314.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:55329905 C>A maps to ENST00000355608 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr19:55341402 G>T maps to NM_013289.2 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr19:55363736 G>T maps to NM_006737.2 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:158057650 G>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:36348352 G>A maps to NM_199180.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:126299111 G>T maps to NM_032531.3 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr11:126333055 G>T maps to NM_032531.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:55564552 C>T maps to NM_000222.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr4:55593613 T>A maps to NM_000222.2 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr2:10192504 G>T maps to NM_003597.4 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:74289589 C>G maps to NM_007249.4 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr13:74269768 C>T maps to NM_007249.4 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:126071006 G>A maps to NM_014079.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:126062659 C>T maps to NM_014079.3 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:44595239 C>T maps to NM_173484.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:44596260 C>A maps to NM_173484.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr4:38691455 C>T maps to NM_016531.5 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr13:73636111 T>G maps to NM_001730.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:56295865 G>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:56296636 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:50176426 G>A maps to NM_172193.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr7:129760628 G>T maps to NM_014997.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:129769364 C>A maps to NM_014997.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr14:50246317 A>G maps to NM_014315.2 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr14:50247036 C>T maps to NM_014315.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:27950783 C>T maps to NM_020782.1 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:18809310 G>A maps to NM_152375.2 W612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr1:161069479 G>C maps to NM_152366.4 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr13:70535577 T>C did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr13:70514186 G>T maps to NM_020866.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr13:70293565 A>C maps to NM_020866.2 Y650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr13:70514309 A>C maps to NM_020866.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr13:70535465 C>T maps to NM_020866.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr13:70456585 G>T maps to NM_020866.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr13:70681660 G>C maps to NM_020866.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr13:70314551 T>A maps to NM_020866.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr13:70281776 G>A maps to NM_020866.2 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr17:40021155 G>T maps to NM_018143.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:117033293 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:30275435 C>T maps to NM_020805.1 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr18:30349715 G>T maps to NM_020805.1 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr18:30350179 C>A maps to NM_020805.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr18:30254621 A>C maps to NM_020805.1 *629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:24006148 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:24024734 C>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr3:47371566 C>T maps to NM_025010.4 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:47374702 C>T maps to NM_025010.4 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr22:20819580 G>A maps to NM_032775.3 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr22:20819554 C>A maps to NM_032775.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr22:20819558 G>T maps to NM_032775.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:183382715 A>G maps to NM_017644.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:183368734 T>C maps to NM_017644.3 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr19:18778680 G>A maps to NM_018316.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:18778776 G>C maps to NM_018316.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:45414768 C>A maps to ENST00000355081 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr5:136963998 G>A maps to NM_017415.2 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:97512601 G>A maps to NM_052904.3 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:97533045 C>T maps to NM_052904.3 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:97561846 T>C maps to NM_052904.3 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:97489366 G>T did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:21675116 G>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:21675229 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:21674688 C>A did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr23:21675150 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:124659170 C>A maps to NM_001081675.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr8:124664914 G>A maps to NM_001081675.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr8:124658215 T>C maps to NM_001081675.2 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:86869435 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:86888804 T>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:86773097 C>A did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr23:86919918 G>T did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:86869559 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:86887306 T>G did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:86888826 G>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:86890575 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:86773048 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr4:39064184 A>G maps to NM_015990.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr4:39083641 C>T maps to NM_015990.4 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:39082827 G>A maps to NM_015990.4 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr3:183209888 G>A maps to NM_130446.2 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:23163418 C>T maps to NM_001031710.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr7:23205372 C>T maps to NM_001031710.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:88116478 G>C maps to NM_020803.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr19:51322497 C>T maps to NM_002257.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:51563313 C>A maps to NM_015596.1 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:51329079 C>T maps to NM_017509.2 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr19:51330014 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:51361392 C>G maps to NM_001648.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:51361742 G>T maps to NM_001648.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:51452187 G>A maps to NM_012427.4 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr19:51471319 C>A did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr19:51483082 C>G maps to NM_005046.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr19:51480875 G>A maps to NM_005046.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:48681799 C>T maps to NM_001135629.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:48688335 C>G maps to NM_001135629.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:48687002 C>T maps to NM_001135629.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr12:9750712 C>T maps to NM_002258.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr12:10601877 C>G maps to NM_213658.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr12:10601871 G>A maps to NM_213658.2 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:10569291 T>A maps to NM_007333.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:10560281 C>A maps to NM_013431.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr12:9984948 G>T maps to NM_016523.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr12:9147763 G>A maps to NM_005810.3 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr7:139164405 G>A maps to NM_198508.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr7:139168178 C>A maps to NM_198508.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:241724046 G>A maps to NM_003679.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:134996994 G>A did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr10:135000075 C>A maps to ENST00000368572 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:186445034 G>T maps to NM_001102416.2 G192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr3:186457172 C>T maps to NM_001102416.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr12:123042028 C>T maps to NM_014708.4 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr12:123060175 G>T maps to NM_014708.4 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr17:66040121 C>T maps to NM_002266.2 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr13:50280448 T>C maps to NM_002267.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:160219933 G>A maps to NM_002268.3 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:160225961 T>C maps to NM_002268.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:160219891 C>T maps to NM_002268.3 *522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:117043287 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:32626220 C>T maps to NM_012316.4 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:152732579 C>T maps to NM_001025231.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:149418624 C>T maps to NM_032534.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:149418507 G>T maps to NM_032534.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:8274696 A>G maps to NM_213597.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:8272808 G>T maps to NM_213597.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:10671753 G>A maps to NM_023008.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:91867068 T>C maps to NM_194456.1 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:91830050 C>T maps to NM_194456.1 *737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:53071126 A>G maps to NM_006121.3 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:53070087 G>A maps to NM_006121.3 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:39020083 G>C maps to NM_000223.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr17:39658977 G>T maps to NM_153490.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr17:39740082 C>A maps to NM_000526.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:39739614 C>T maps to NM_000526.4 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:39768835 C>A maps to NM_005557.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr17:39767162 C>A maps to NM_005557.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:39768814 G>T maps to NM_005557.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr17:39778624 C>A maps to NM_000422.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr12:53345368 C>T maps to NM_000224.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:53045529 C>A maps to NM_000423.2 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:53044193 G>C maps to NM_000423.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:39034578 G>T maps to NM_019010.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:38816288 C>A maps to NM_152349.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr17:38812816 A>T maps to NM_152349.2 L242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr17:39525756 C>T maps to ENST00000394004 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:39521218 G>A maps to ENST00000394004 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:39535404 C>T maps to NM_021013.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr17:39635145 G>T maps to NM_002280.4 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:39578371 C>T maps to NM_003770.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:39578434 G>A maps to NM_003770.4 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:39578671 C>T maps to NM_003770.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:39122795 C>A maps to NM_213656.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:39116540 C>T maps to NM_213656.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:52913696 A>G maps to NM_000424.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:52913993 G>A maps to NM_000424.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr12:52913972 G>C maps to NM_000424.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr12:52882245 C>A maps to NM_005554.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr12:52841593 G>T maps to NM_005555.3 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr12:52979816 G>A maps to NM_080747.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:52992805 C>A maps to NM_080747.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:53008395 T>A maps to NM_175068.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:53008427 C>A maps to NM_175068.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:52967270 C>A maps to NM_175053.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr12:53091604 C>A maps to NM_175078.2 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:53096843 C>G maps to NM_175078.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:53233570 C>T maps to NM_173352.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:53227801 C>T maps to NM_175834.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr12:53298546 C>T maps to NM_002273.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:52680956 C>G maps to NM_002281.3 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr12:52715020 G>T maps to NM_002282.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:52774240 G>A maps to NM_033045.3 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr12:52774340 G>A maps to NM_033045.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:52758918 C>T maps to NM_002283.3 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:52760964 G>T maps to NM_002283.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr12:52760913 G>T maps to NM_002283.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr17:39724765 G>T maps to NM_000226.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:39197319 T>C maps to NM_030967.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr17:39190671 G>T maps to NM_030966.1 C134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr17:39190914 A>G maps to NM_030966.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:46117565 C>T maps to NM_198699.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr21:46117424 C>A maps to NM_198699.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr21:46117823 C>A maps to NM_198699.1 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr21:45999819 G>A maps to NM_198694.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:45999862 G>T maps to NM_198694.2 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr21:46011354 C>T maps to NM_198688.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr21:46020943 C>A maps to ENST00000380102 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr21:46047882 C>A maps to NM_198690.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr21:46086488 G>A maps to NM_181684.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr21:46078015 C>A maps to NM_198697.2 C40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr21:46078054 C>A maps to NM_198697.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr21:31768610 C>T maps to NM_181599.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr21:31768853 C>T maps to NM_181599.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr21:31744282 G>T maps to NM_181621.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr21:31744141 C>A maps to NM_181621.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr21:31744282 G>A maps to NM_181621.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr21:31798005 G>A maps to NM_181622.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr21:31798086 C>A maps to NM_181622.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr21:31802904 G>T maps to NM_181600.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr21:31802739 G>A maps to NM_181600.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr21:31802907 G>T maps to NM_181600.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr21:31864182 G>A maps to NM_181609.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr21:31914083 A>G maps to ENST00000437381 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr21:32119450 C>A maps to NM_181617.1 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr21:31709363 C>T maps to NM_001077711.1 *208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr21:31709431 G>T maps to NM_001077711.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr17:39305581 G>T maps to NM_033188.3 C146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:71293712 A>T maps to ENST00000376535 C57*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3406-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:1651540 C>T maps to NM_001001480.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr11:1718723 T>A maps to NM_001012416.1 C83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:1718687 C>A maps to NM_001012416.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr11:71238459 C>A maps to NM_001012503.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr21:31986058 G>A maps to NM_181602.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr21:31986181 G>T maps to NM_181602.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr21:31964913 C>G maps to NM_181605.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:39406115 C>A maps to ENST00000431129 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr17:25938600 C>T maps to ENST00000268763 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:25924358 A>T maps to ENST00000268763 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:117977638 C>G maps to ENST00000339824 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr12:118199245 C>A maps to ENST00000339824 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:117963024 C>T did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:52498724 C>A maps to NM_138417.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr14:56096778 T>C maps to NM_001079521.1 H395H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:56117285 G>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:134322633 G>C maps to NM_178554.4 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:134322711 C>T maps to NM_178554.4 W565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:134339654 G>C maps to NM_178554.4 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:134362193 G>A maps to NM_178554.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:143798133 G>T maps to NM_003937.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:153136335 G>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:153130846 G>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:153137709 G>T did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr23:153136599 G>T did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:153132841 C>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:62675519 A>T maps to NM_019079.4 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr22:41605723 G>T maps to NM_031488.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:130454628 C>T maps to NM_032438.2 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:130370464 A>G maps to NM_032438.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:130392203 G>T maps to NM_032438.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr18:5969550 C>A maps to NM_173464.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:6237992 C>A maps to NM_173464.3 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:6886552 C>G maps to NM_002286.5 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:153706633 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:153706718 C>T did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:54867017 C>A maps to NM_002287.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr19:54867876 C>A did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr19:55019215 G>T maps to NM_002288.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr19:55019391 G>C maps to NM_002288.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr18:6949174 T>C maps to NM_005559.2 G2827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr18:6971893 A>G maps to NM_005559.2 Y2287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr18:6997881 G>T maps to NM_005559.2 S1555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr18:7049208 T>A maps to NM_005559.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr18:6999567 C>A maps to NM_005559.2 P1513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr18:6975959 G>A maps to NM_005559.2 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr18:6993638 C>T did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr18:6986249 T>A maps to NM_005559.2 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:129468138 G>C maps to NM_000426.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr6:129470192 C>T maps to NM_000426.3 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:129828632 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:129674446 A>G maps to NM_000426.3 G1554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:129807695 T>A maps to NM_000426.3 I2609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:129513970 C>T maps to NM_000426.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr6:129826501 T>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:129712690 C>T maps to NM_000426.3 A1709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:129674307 G>T did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr6:129649433 G>T maps to NM_000426.3 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:129691051 C>T maps to NM_000426.3 Q1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:129759878 T>G maps to NM_000426.3 T2019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:129419419 C>T maps to NM_000426.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr18:21424983 A>G maps to ENST00000416669 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr18:21531684 C>A maps to ENST00000416669 S3229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr18:21534554 C>A maps to ENST00000416669 V3317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr18:21501540 C>T maps to ENST00000416669 I2725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr18:21427527 A>G maps to ENST00000416669 S1346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr6:112463332 G>A maps to NM_001105206.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:112451159 T>A maps to NM_001105206.1 K1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:112462012 C>T maps to NM_001105206.1 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:112486415 C>G maps to NM_001105206.1 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:112486383 G>T maps to NM_001105206.1 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr6:112462045 C>A maps to NM_001105206.1 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:60885613 G>A maps to NM_005560.3 F3487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr20:60908747 G>A maps to NM_005560.3 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr20:60903445 C>T maps to NM_005560.3 P1501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr20:60885756 G>T maps to NM_005560.3 G3470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr20:60895860 G>A maps to NM_005560.3 G2194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr20:60905966 C>T maps to NM_005560.3 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr20:60893578 C>A maps to NM_005560.3 R2390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr20:60893680 C>G maps to NM_005560.3 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr20:60893953 C>T maps to NM_005560.3 R2329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr7:107621202 C>A maps to NM_002291.2 G244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr7:107615433 G>A maps to NM_002291.2 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:49160960 C>A maps to NM_002292.3 E1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:209799240 C>A maps to NM_000228.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:209791920 G>A maps to NM_000228.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr7:107692542 C>T maps to NM_007356.2 A1305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:183087213 T>C maps to NM_002293.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr1:183086558 C>A maps to NM_002293.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:183204742 G>A maps to NM_005562.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:183200119 C>G maps to NM_005562.2 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:183177131 G>T maps to NM_005562.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr9:133942458 C>T maps to ENST00000355048 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr9:133962939 G>T maps to ENST00000355048 T1448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr9:133914548 C>A maps to ENST00000355048 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr9:133901777 C>A maps to ENST00000355048 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:119575624 C>T did not map to a codon.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:182841949 G>T maps to NM_014398.3 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr7:55468868 A>G maps to NM_018697.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:37526616 C>G did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:17590573 T>C maps to NM_015907.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:17581490 G>T maps to NM_015907.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:31208106 G>T maps to NM_006762.2 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr22:34046523 G>A maps to NM_133642.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr22:34000432 T>C maps to NM_133642.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:930415 G>A maps to NM_015155.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr10:871189 T>C maps to NM_015155.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr10:863799 T>C maps to NM_015155.1 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr15:71124720 C>T maps to NM_018357.2 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr4:113565912 C>T maps to ENST00000509061 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:113575315 G>T did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr4:113568939 A>G maps to ENST00000509061 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr5:145493752 C>A maps to NM_020117.9 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:145537058 G>A maps to NM_020117.9 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:45588956 C>T maps to NM_015340.3 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:64737900 T>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:64738140 C>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:64734719 G>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:64748147 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:64738215 C>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:64749616 A>C did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:64753612 G>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:64749593 G>C did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr23:64749608 T>C did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:18995019 C>A maps to NM_021267.3 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:101024833 C>A maps to ENST00000394113 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr15:101009682 T>A maps to ENST00000394113 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr15:100996211 G>C maps to ENST00000394113 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:149983368 G>A maps to NM_004690.2 I963I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:150004301 G>A maps to NM_004690.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr6:150004706 T>C maps to NM_004690.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr6:150005648 C>A maps to NM_004690.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:21563270 G>A maps to NM_014572.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:203740493 G>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:111430954 G>A maps to ENST00000375615 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:225607145 G>A maps to NM_194442.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:225599053 G>A maps to NM_194442.1 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:102987413 G>A maps to NM_006562.4 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr10:102987050 G>A maps to NM_006562.4 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:80228524 C>T maps to NM_181714.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:67976607 C>T maps to NM_000229.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:152759780 C>G maps to NM_178353.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:152748936 C>A maps to ENST00000439693 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr16:25186342 G>T maps to ENST00000380963 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr15:43621301 C>G maps to NM_014793.4 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:43621184 T>A maps to NM_014793.4 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr9:138416975 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:46708348 G>A maps to NM_002298.4 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr13:46730702 C>A maps to NM_002298.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:169697831 G>T maps to NM_005565.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:136566199 C>A maps to NM_002299.2 S1239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:136566580 G>T maps to NM_002299.2 Y1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:136570430 C>T maps to NM_002299.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:136552209 C>A did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr2:136547234 G>T maps to NM_002299.2 I1823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:136594715 G>C maps to NM_002299.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:136575531 G>T maps to NM_002299.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr2:136562336 C>T maps to NM_002299.2 Q1488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr15:66857145 G>A maps to NM_207338.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:16504480 C>A maps to NM_001290.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:16597388 G>C maps to NM_001290.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:88441530 G>A maps to NM_001171610.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr10:88451676 C>A maps to NM_001171610.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:88441530 G>T maps to NM_001171610.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:88485897 C>A maps to NM_001171610.1 Y666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr15:59499576 T>A maps to NM_033195.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:21788640 C>A maps to NM_002300.6 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:21788613 G>A maps to NM_002300.6 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr16:75146774 G>T maps to NM_153486.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr16:75148011 C>G maps to NM_153486.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:36248659 G>T maps to NM_174902.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr11:36248917 G>A maps to NM_174902.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:36057728 G>A maps to NM_174902.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:140271149 C>G did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr13:53307422 C>T maps to NM_007015.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr13:53307397 C>A maps to NM_007015.2 G104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:226125167 C>A maps to NM_003240.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:226125442 C>A maps to NM_003240.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr12:65633947 G>T maps to NM_014319.4 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:65632463 C>T maps to NM_014319.4 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:65633914 G>C did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr12:65564641 C>T maps to NM_014319.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:154966200 C>T maps to NM_018655.2 Q40*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-46-6026-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:54974004 G>A maps to NM_198988.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr19:54973314 C>T maps to NM_198988.1 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:66067349 G>T maps to NM_002303.5 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr1:66102464 G>T maps to NM_002303.5 E1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:66102685 C>T maps to NM_002303.5 D1162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:66064401 G>T maps to NM_002303.5 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:43213038 T>A maps to NM_022356.3 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:43224592 T>A maps to NM_022356.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:65897502 C>A maps to NM_017526.4 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:65895677 G>T maps to NM_017526.4 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr4:1821199 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:38257910 C>A maps to ENST00000379957 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:2565316 A>T did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr11:63278577 G>C did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr19:40097909 G>A maps to NM_013268.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr19:40097948 C>T maps to NM_013268.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:76967756 C>A maps to NM_005567.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:39297205 C>T maps to NM_006149.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr10:95518044 T>A maps to NM_005097.2 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr10:95518035 G>A maps to NM_005097.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:95557190 G>T maps to NM_005097.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr4:25026480 G>C maps to NM_018176.3 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr4:25005390 G>T maps to NM_018176.3 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:27390142 C>T maps to NM_018490.2 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr11:27390516 A>G maps to NM_018490.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:27402513 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:71978099 G>T maps to NM_003667.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:202273704 C>A maps to NM_001017403.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:63995608 A>G maps to NM_016571.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:64004920 A>G maps to NM_016571.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:206784716 G>A maps to NM_006893.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:48915113 G>A maps to NM_000233.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:48925803 C>A maps to NM_000233.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:48915006 G>T maps to NM_000233.3 C643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:48925887 G>T maps to NM_000233.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr2:48915453 A>G maps to NM_000233.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:111903880 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:111914543 G>T did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:111914293 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr7:103969485 G>T maps to NM_199000.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:35782500 C>T maps to NM_182548.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr10:126172722 G>A maps to NM_022126.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:126783546 C>G maps to NM_004789.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:180235535 C>A maps to NM_033343.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:75606779 T>A maps to NM_001001933.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr22:30640023 G>T maps to NM_002309.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:48624465 G>T maps to NM_000234.1 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:33323663 G>A maps to NM_013975.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:33319586 C>A maps to NM_013975.3 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:108862305 G>A maps to NM_001098268.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr13:108862404 C>T maps to NM_001098268.1 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr13:108863507 T>A maps to NM_001098268.1 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr13:108861231 C>A maps to NM_001098268.1 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:55106307 C>T maps to NM_006863.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:55098689 G>A maps to NM_001130917.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:55086891 C>T maps to NM_001130917.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:55086420 G>A maps to NM_001130917.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr19:55087568 G>T maps to NM_001130917.1 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:55086321 A>G maps to NM_001130917.1 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:55087508 C>A maps to NM_001130917.1 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:55085813 C>T maps to NM_001130917.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:54802092 G>A maps to ENST00000251375 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:54803247 G>A maps to ENST00000251375 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:54849796 C>A maps to NM_012276.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:54849408 C>T maps to NM_012276.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:54848833 G>A maps to NM_012276.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:54823221 T>C maps to NM_021250.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:54744734 G>A maps to ENST00000245620 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr19:54745536 C>T maps to ENST00000270464 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:54742960 T>C maps to NM_024318.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:54744148 C>A did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:54744725 G>A maps to ENST00000245620 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:55143128 C>T maps to ENST00000427581 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:55148199 C>A maps to ENST00000427581 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:55144656 C>A maps to ENST00000427581 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:55143119 G>A maps to ENST00000427581 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr19:55143938 C>G maps to ENST00000427581 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr19:55144572 C>T maps to ENST00000427581 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr19:55144518 C>A maps to ENST00000427581 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:55147044 G>A maps to ENST00000427581 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:54782922 A>G maps to ENST00000391747 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:54783385 C>A maps to ENST00000391747 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:54782141 G>A maps to ENST00000391747 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:54780733 G>T maps to ENST00000391747 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:54782787 C>T maps to ENST00000391747 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:54780769 G>A maps to ENST00000391747 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:54724575 C>T maps to NM_001081450.1 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:55179358 C>T maps to ENST00000391733 Y413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr19:55179346 G>A maps to ENST00000391733 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:55175366 G>T maps to ENST00000391733 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:55179208 A>C maps to ENST00000391733 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:54760032 G>A maps to NM_001081442.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:54758730 A>G maps to NM_001081442.1 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:45637321 G>T maps to NM_014240.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:109276213 C>T maps to NM_001193484.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:128398511 C>A maps to NM_017980.4 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:105526585 C>A maps to NM_001004317.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr19:36245291 A>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:81205390 C>A maps to NM_004664.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr15:77906691 G>C maps to NM_032808.5 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr15:77908026 G>C maps to NM_032808.5 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr15:77907009 C>T maps to NM_032808.5 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr15:77907684 G>A maps to NM_032808.5 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr9:27949202 A>T maps to NM_152570.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr9:27949217 G>T maps to NM_152570.1 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:58855730 G>T maps to NM_000236.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:42911518 C>A maps to NM_005357.2 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:42910325 G>C maps to NM_005357.2 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr18:47088746 A>C maps to NM_006033.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr21:15481334 T>G maps to NM_198996.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr21:15558280 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr21:15554097 G>C maps to NM_198996.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr21:15554142 T>A maps to NM_198996.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:90356156 G>A maps to NM_001010939.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:11650520 G>A maps to NM_001136472.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr15:75108844 C>A maps to NM_021819.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr5:176764784 C>T maps to NM_006816.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:49495908 C>A maps to NM_018113.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:36136479 C>G maps to NM_001007527.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:197717442 C>T maps to NM_001136049.2 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:156084924 C>A maps to NM_170707.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:76415913 G>T maps to ENST00000357063 E1206*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-33-4566-01A-01D-1441-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr13:76427225 A>T did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:201915417 G>A maps to NM_012134.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:201915296 G>A maps to NM_012134.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:201868375 G>A maps to NM_012134.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:123296223 G>T maps to NM_207163.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr7:97822521 G>T maps to NM_014916.3 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr7:97823670 G>T maps to NM_014916.3 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr7:97823673 G>A maps to NM_014916.3 R1299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:97822170 C>A maps to NM_014916.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr19:49001463 T>C maps to NM_001080434.1 R983R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:165322359 G>A maps to NM_177398.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr9:129455562 C>T maps to NM_001174147.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:129458163 G>T maps to NM_001174147.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:100170717 C>A maps to ENST00000489752 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr5:96332122 G>A maps to NM_005575.2 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:54343059 C>G maps to NM_001126328.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:19257869 T>A maps to ENST00000410050 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:5692043 C>T maps to NM_004793.2 *960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:12583330 G>A maps to NM_152271.3 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:100906845 G>A maps to NM_198461.3 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:100906842 C>G maps to NM_198461.3 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:100938033 C>A maps to NM_198461.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr2:100915387 C>G maps to NM_198461.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:118116785 A>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:118109536 A>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:118123388 C>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:118124509 G>A did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:118147104 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:118143098 C>G did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr15:74239500 C>T maps to NM_005576.2 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:74761090 T>A maps to NM_032603.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:161015039 G>C maps to NM_005577.2 S1193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:161022045 C>T maps to NM_005577.2 E1010E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:161071442 C>A maps to NM_005577.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:160953574 A>G maps to NM_005577.2 T1983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:161007643 G>T maps to NM_005577.2 Y1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr19:19737829 G>A maps to NM_004720.5 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:19735129 C>A maps to NM_004720.5 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:78011399 C>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:78010793 C>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:78010583 A>T did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:78011259 C>A did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:78010450 A>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:78010546 C>G did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:1463864 T>C maps to NM_024830.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:1479780 G>A maps to NM_024830.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr5:1489887 C>A maps to NM_024830.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr15:34656451 T>A maps to NM_153613.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:212002482 C>T maps to NM_014873.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:211952258 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:14266333 C>T maps to NM_001008701.2 W1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:14263175 G>A maps to NM_001008701.2 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr19:14273820 G>A maps to NM_001008701.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:14273976 C>A maps to NM_001008701.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:82408776 C>T maps to ENST00000370717 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:62542558 C>A maps to ENST00000506720 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:62758437 A>G maps to ENST00000506720 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr4:62453083 T>C maps to ENST00000506720 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr2:11911569 A>T maps to ENST00000396099 K127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr20:39978996 A>T maps to NM_022896.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr8:19809326 G>A maps to NM_000237.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:19805769 C>G maps to NM_000237.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:56320360 C>G maps to NM_006151.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr17:56344881 T>C maps to NM_006151.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:188584085 G>C maps to NM_005578.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:104048414 C>T maps to NM_017753.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:11474412 C>T maps to NM_001170635.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:99771996 C>T maps to NM_014839.4 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:99771995 C>A maps to NM_014839.4 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:99771401 C>T maps to NM_014839.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr1:99772301 G>C maps to NM_014839.4 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr4:151336616 T>C maps to NM_006726.3 S2400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr4:151771879 T>A maps to NM_006726.3 R1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr4:151752972 G>C maps to NM_006726.3 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:151773087 C>T maps to NM_006726.3 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:114357363 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:114422789 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:197566205 G>A maps to ENST00000425562 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:100174906 C>T maps to NM_002319.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:803519 C>T maps to NM_145886.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:39805490 G>A maps to NM_020862.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr19:39805145 C>T maps to NM_020862.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr6:40399553 G>A maps to NM_020737.1 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:40400369 G>C maps to NM_020737.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr6:40400483 C>A maps to NM_020737.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:40399928 G>A maps to NM_020737.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:66626555 C>T maps to NM_024036.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr14:42360884 C>A maps to NM_152447.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr14:42356394 G>A maps to NM_152447.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr14:42360907 C>A maps to NM_152447.3 S614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr14:42360791 G>T maps to NM_152447.3 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr14:42361007 T>A maps to NM_152447.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr14:42357018 C>T maps to NM_152447.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr14:42356067 G>T maps to NM_152447.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr7:133812131 C>G maps to NM_144648.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:133821795 G>C maps to NM_144648.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:133812167 C>A maps to NM_144648.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr7:133859318 G>A maps to NM_144648.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:66431073 C>T maps to NM_015541.2 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:66502050 G>C maps to NM_015541.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:66436510 G>T maps to NM_015541.2 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:113616219 G>T maps to NM_014813.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:113661919 C>T maps to NM_014813.1 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:113666600 G>T maps to NM_014813.1 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:113657151 C>T maps to NM_014813.1 N728N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:59274432 C>A maps to NM_153377.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr12:59274486 C>A maps to NM_153377.3 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:59276649 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr12:59271447 G>T maps to NM_153377.3 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:85991970 G>A maps to NM_015613.2 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr10:85992084 G>T maps to NM_015613.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr4:110791572 A>T maps to NM_198506.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr12:25243094 G>A maps to ENST00000354454 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:57593028 G>A maps to NM_002332.2 L3237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr12:57573259 G>A maps to NM_002332.2 V1629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr12:57593148 C>T maps to NM_002332.2 D3277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr12:57595585 G>T maps to NM_002332.2 E3498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr12:57594584 C>T maps to NM_002332.2 D3404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:57588393 C>T maps to NM_002332.2 F2701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr14:23346450 G>A maps to NM_014045.3 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr14:23342529 C>T maps to NM_014045.3 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr14:23342655 G>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:105502955 A>T maps to NM_013437.4 L842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:105509435 G>A maps to NM_013437.4 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:141771262 C>A maps to NM_018557.2 G748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr2:141457888 G>T maps to NM_018557.2 Y2243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:141359116 A>T maps to NM_018557.2 T2297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:141643895 C>A maps to NM_018557.2 E1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:141128386 C>A maps to NM_018557.2 E3634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr2:141473549 T>A maps to NM_018557.2 P2005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:141253290 C>A maps to NM_018557.2 L2959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:141819823 G>A maps to NM_018557.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:141986914 T>A maps to NM_018557.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:141707966 G>A maps to NM_018557.2 D991D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr2:142004810 A>T maps to NM_018557.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:141459803 C>A maps to NM_018557.2 E2070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:142012190 T>C maps to NM_018557.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:141274520 A>G maps to NM_018557.2 L2696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:141806618 G>A maps to NM_018557.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:141083358 A>G maps to NM_018557.2 N4104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:141201952 A>G maps to NM_018557.2 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr2:141598638 T>C maps to NM_018557.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr2:141072663 A>G maps to NM_018557.2 D4215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:141474322 G>A maps to NM_018557.2 Q1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:141773276 C>T maps to NM_018557.2 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:141260666 G>T maps to NM_018557.2 R2843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:141250259 C>A maps to NM_018557.2 E3013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:170003309 C>T maps to NM_004525.2 K4250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:170127412 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:170150709 A>G maps to NM_004525.2 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:170012823 C>T maps to NM_004525.2 T4037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr2:170013974 G>A maps to NM_004525.2 C3975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr2:170058364 G>T maps to NM_004525.2 S2742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:170042515 G>A maps to NM_004525.2 C3114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:170059404 C>T maps to NM_004525.2 K2690K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:169993937 G>A maps to NM_004525.2 A4528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:170127510 A>G maps to NM_004525.2 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:170042266 G>A maps to NM_004525.2 I3197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr2:170030451 G>T maps to NM_004525.2 S3664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:170063380 G>A maps to NM_004525.2 I2283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:170012910 G>A maps to NM_004525.2 I4008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:170097687 G>A maps to NM_004525.2 H1285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr2:170038678 A>T maps to NM_004525.2 Y3332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr2:170127501 G>A maps to NM_004525.2 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:170103422 G>A maps to NM_004525.2 F994F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:170070376 C>A maps to NM_004525.2 E1944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:33698453 C>T maps to NM_002333.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr11:46903276 A>G maps to ENST00000256991 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:46900683 C>T maps to ENST00000256991 R1044R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:68115651 G>A maps to NM_002335.2 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:68190985 C>G maps to NM_002335.2 G1019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr11:68205912 G>C did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:68174199 G>T maps to NM_002335.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:68204450 C>T maps to NM_002335.2 S1365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:68191057 G>A maps to NM_002335.2 E1043E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:12291457 C>T maps to NM_002336.2 R1136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr12:12336940 G>A maps to NM_002336.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:12303937 A>G maps to NM_002336.2 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:53728157 C>A maps to NM_004631.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:3514745 C>T maps to NM_002337.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:44115752 C>A maps to NM_133259.3 E1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:44139578 C>G maps to NM_133259.3 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr12:70003883 T>C maps to NM_201550.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:145746732 C>T maps to NM_014665.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr8:145745720 A>G maps to NM_014665.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:194080932 G>A maps to NM_001135057.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:194080710 C>T maps to NM_001135057.2 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:194080602 G>C maps to NM_001135057.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr6:25450633 A>G maps to NM_017640.5 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:24528917 G>A maps to NM_138360.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:24524986 C>T maps to NM_138360.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr14:24524478 C>A maps to NM_138360.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:24522925 C>A maps to NM_138360.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr7:102574464 G>C maps to NM_001031692.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:46574381 T>A maps to NM_024512.3 K170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr3:46569046 G>C maps to NM_024512.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr10:72061169 C>T maps to NM_207119.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:67241849 G>T maps to NM_001004055.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr18:7231414 G>C maps to NM_001105581.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr18:7231498 C>G maps to NM_001105581.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:76372513 G>C maps to NM_001128922.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:196387953 C>A maps to NM_198565.1 C480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr3:196381478 C>T maps to NM_198565.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:196386966 C>T maps to NM_198565.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr3:196386690 C>A maps to NM_198565.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:62855862 C>T maps to NM_199340.2 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr17:62856036 T>C maps to NM_199340.2 P1409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr17:62856605 G>A maps to NM_199340.2 Q1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:26751351 T>A maps to NM_052953.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:70639151 G>T maps to NM_017768.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:46763300 G>A maps to ENST00000254454 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:122685423 C>T maps to NM_001098519.1 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr12:122669154 G>T maps to NM_001098519.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:45914173 G>A maps to NM_033413.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr15:71211505 T>C maps to NM_017691.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr15:71341746 G>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr15:71272437 A>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:40137000 A>T maps to NM_020929.1 L281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr11:40136636 C>A maps to NM_020929.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr16:84193348 C>T maps to NM_178452.4 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:165532886 C>T maps to NM_001005214.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:56949825 C>A maps to NM_001005210.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:56949948 G>A maps to NM_001005210.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:56949612 C>G maps to NM_001005210.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr11:551688 G>T maps to NM_198075.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr15:42839476 G>C maps to NM_153260.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:133673829 A>G maps to ENST00000250173 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:52864045 G>A maps to NM_001024611.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:52883287 G>A maps to NM_001024611.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:70503936 G>C maps to NM_020794.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:70541816 G>T maps to NM_020794.2 E1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:70446060 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:70226033 G>A maps to NM_020794.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:70291483 G>T maps to NM_020794.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:70502166 G>T maps to NM_020794.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:70573481 A>G maps to NM_020794.2 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:70397237 T>C maps to NM_020794.2 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr9:131670129 G>T maps to NM_001127244.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:90048539 G>T maps to NM_015350.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:90179548 C>T maps to NM_032270.4 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:7965540 G>T maps to NM_025061.3 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr8:86044013 G>T maps to NM_033402.4 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:86047239 G>A maps to NM_033402.4 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr8:86027431 A>G maps to NM_033402.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr8:86050584 G>C maps to NM_033402.4 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:238672185 G>A maps to NM_001137552.1 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:238661984 A>T maps to NM_001137552.1 K173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:85515540 A>T maps to NM_001079910.1 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr12:85450480 C>A maps to NM_001079910.1 S637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:85546833 A>T maps to NM_001079910.1 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr12:85441058 G>T maps to NM_001079910.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr12:85547825 G>A maps to NM_001079910.1 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:85441103 G>A maps to NM_001079910.1 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:74492583 G>A maps to NM_001105659.1 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:74507324 T>C maps to NM_001105659.1 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:74507363 G>T maps to NM_001105659.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr1:74648473 A>G maps to NM_001105659.1 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:74507258 T>C maps to NM_001105659.1 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:74648473 A>G maps to NM_001105659.1 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:74507459 G>T maps to NM_001105659.1 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:169546551 T>C maps to NM_001080460.1 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr3:169539957 G>T maps to NM_001080460.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr3:169548371 G>A maps to NM_001080460.1 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr3:169546578 G>T maps to NM_001080460.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:169540077 C>T maps to NM_001080460.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr3:169540308 A>T maps to NM_001080460.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:169540419 G>C maps to NM_001080460.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:169540062 C>T maps to NM_001080460.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:101528974 C>T maps to NM_024652.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:101565078 C>T maps to NM_024652.3 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:101597158 C>A maps to NM_024652.3 S1477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:101554531 C>T maps to NM_024652.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:40761489 G>T maps to NM_198578.3 E2503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:40728878 T>C maps to NM_198578.3 D1956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:40740725 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:40689241 T>G maps to NM_198578.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:40703025 C>T maps to NM_198578.3 F1436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:40629430 G>A maps to NM_198578.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:40753183 G>A maps to NM_198578.3 K2322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:40760847 G>T maps to NM_198578.3 R2477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:3887224 C>T maps to NM_020873.5 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:204588133 G>A maps to NM_201630.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:110764816 G>A maps to NM_018334.4 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr7:110763553 T>G maps to NM_018334.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:110763986 C>T maps to NM_018334.4 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:110763775 T>C maps to NM_018334.4 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:80530587 C>A maps to NM_178839.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:80530770 G>C maps to NM_178839.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:80529501 A>G maps to NM_178839.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:80530674 C>T maps to NM_178839.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:80529579 G>T maps to NM_178839.4 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr2:80529585 G>A maps to NM_178839.4 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:80530488 G>T maps to NM_178839.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:80529459 G>A maps to NM_178839.4 N495N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:80529903 G>T maps to NM_178839.4 Y347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:80529774 C>A maps to NM_178839.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:80530053 G>C maps to NM_178839.4 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr10:68686703 C>T maps to NM_178011.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr2:77746265 G>A maps to NM_001134745.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:77746910 C>A maps to NM_001134745.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:77745533 G>A maps to NM_001134745.1 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:77745748 C>A maps to NM_001134745.1 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:77746835 T>G maps to NM_001134745.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:77746748 G>T maps to NM_001134745.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:77746337 C>T maps to NM_001134745.1 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr2:77745860 G>T maps to NM_001134745.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:77746049 G>A maps to NM_001134745.1 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:77745791 T>A maps to NM_001134745.1 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:77745842 G>A maps to NM_001134745.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:76975850 C>T maps to NM_001134745.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr9:130258288 C>A maps to NM_001005374.2 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr12:1943682 C>T maps to NM_001163926.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr11:71806463 C>T maps to NM_145309.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:115560809 C>T maps to NM_002338.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr3:115560722 C>A maps to NM_002338.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr19:34712410 G>C did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr20:60699679 C>T maps to NM_144703.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr19:35757274 C>A maps to NM_205834.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr12:21207462 A>T maps to ENST00000381541 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:21229442 G>A maps to ENST00000381541 W576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:21205081 G>T maps to ENST00000381541 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:21172203 T>C maps to ENST00000381541 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr12:21200044 T>A maps to ENST00000381541 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr12:21196274 C>T maps to ENST00000381541 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr12:21205155 A>G maps to ENST00000381541 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:21242883 A>G maps to ENST00000381541 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:31548596 G>C maps to NM_002341.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr2:33518260 A>T maps to ENST00000354476 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:33413797 T>A maps to ENST00000354476 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:33623584 T>C maps to ENST00000354476 N1714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:33335711 C>G maps to ENST00000354476 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr2:33505113 G>T maps to ENST00000354476 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:33567902 A>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:33500941 G>T maps to ENST00000354476 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:33623566 G>A maps to ENST00000354476 P1708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:74972769 G>A maps to NM_000428.2 C1386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:65308029 C>T maps to NM_001130144.2 V1011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:41115448 C>A maps to ENST00000308370 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:46480789 T>C maps to NM_002343.3 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:46491503 C>T maps to NM_002343.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:144183252 G>A maps to NM_032860.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr17:48824019 C>T maps to ENST00000393227 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:23420349 G>A maps to NM_001142546.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:25004677 C>T maps to NM_001009909.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:114541190 C>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:31644734 T>A maps to NM_025262.3 *151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:143784554 T>C maps to ENST00000292430 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:6654802 G>A maps to NM_004271.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:160784492 C>T maps to ENST00000263285 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:160789113 C>G maps to ENST00000263285 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:99863223 G>A maps to NM_175735.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:56879272 G>T did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr8:143831823 G>T maps to NM_205545.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:42342204 G>A maps to NM_173506.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:89815271 G>A maps to NM_198273.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:235840489 T>A did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:235972253 G>A maps to NM_000081.2 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:235972329 G>C maps to NM_000081.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:235945291 G>T maps to NM_000081.2 S1653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:235969540 A>T maps to NM_000081.2 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:235944339 G>C maps to NM_000081.2 S1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:235827886 C>G maps to NM_000081.2 V3691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:235969139 G>T maps to NM_000081.2 S1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:235892929 T>C maps to NM_000081.2 A3024A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr10:29581496 G>C maps to NM_032517.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr10:29578105 A>T maps to NM_032517.4 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:30918577 G>A maps to NM_183058.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr22:21348290 C>A maps to NM_006767.3 R478R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-66-2780-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr13:36049897 G>A maps to NM_005584.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:20198759 A>G maps to NM_182762.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr7:20197948 C>A maps to NM_182762.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:39800236 G>A maps to ENST00000289893 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:39903522 C>T maps to ENST00000361689 I3962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:39927684 C>A maps to ENST00000361689 T5159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr1:39789863 G>C did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr1:39788296 G>A maps to ENST00000361689 L1354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr1:39797857 A>G maps to ENST00000289893 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:39783070 C>T maps to ENST00000361689 L1263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:39910347 G>A maps to ENST00000361689 Q4423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:39798691 G>A maps to ENST00000289893 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:39851506 C>G maps to ENST00000361689 L2688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr1:39927567 C>T maps to ENST00000361689 T5120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:39757595 A>T maps to ENST00000361689 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:39797467 G>T maps to ENST00000289893 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:39945558 C>T maps to ENST00000361689 R5262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:39800458 C>T maps to ENST00000289893 D1173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:39798769 T>C maps to ENST00000289893 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:39914333 G>A maps to ENST00000361689 L4660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:39801334 A>G maps to ENST00000289893 K1465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr11:63767112 C>A did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr20:13982994 C>T maps to ENST00000310348 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr7:2255828 C>A maps to NM_003550.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:47311833 C>A maps to NM_003682.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:47305938 G>C maps to NM_003682.3 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:47296438 G>T maps to NM_003682.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:47312321 C>T maps to NM_003682.3 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr11:47307068 C>A maps to NM_003682.3 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:166962034 C>A maps to NM_032858.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:166974347 G>A maps to NM_032858.1 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr16:79633670 G>A maps to NM_005360.4 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:145160624 C>T maps to NM_032272.4 N13N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr22:38609892 A>G maps to NM_012323.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr19:35804197 G>A maps to NM_002361.3 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr19:35802818 A>G did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr19:35804239 T>G maps to NM_002361.3 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:152483000 C>G did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:152482622 C>T did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:151303873 C>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:151303812 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:151303346 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:148796225 C>G did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:148797857 C>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:148797849 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:148798396 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:148797510 C>T did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:148797278 G>T did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:148797502 C>A did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr23:151900252 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:151900644 C>G did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:151900149 A>G did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:151900624 G>A did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr23:151900356 A>G did not map to a codon.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr23:151935728 G>C did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:151935779 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:151935415 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:151093078 G>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:151092422 C>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:151092184 G>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:151092211 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:151092695 A>G did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:151092291 G>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:151870129 G>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:151870030 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:151870147 G>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:151870229 G>C did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:151870166 T>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:151869604 C>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:151869552 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:151870214 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:151870216 C>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr23:151869720 G>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:151870095 C>T did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:149013523 T>C did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:149013144 T>C did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:30269564 T>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:30269104 G>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:30269092 T>G did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr23:30268616 C>T did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr23:27839467 C>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:27839976 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:35820349 G>A did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:35820594 T>C did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:35820882 T>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:35820580 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:26157986 C>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:26157960 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:26157750 G>T did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:26157220 C>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:26158005 T>G did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:26157144 C>A did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:26157184 C>A did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:30237486 C>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:30237171 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:30237314 T>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:30236722 T>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:30237315 C>A did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:30236740 G>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:30236957 C>G did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:30237232 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:30236735 G>C did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:30237094 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:30254994 C>A did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:30260684 G>T did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:30260616 A>G did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:30260891 T>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:30261045 C>A did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:30261247 T>C did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:30261063 T>C did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:30260359 A>G did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:26212606 C>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:26212946 T>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:26212376 T>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:26212736 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:26212892 C>G did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:26213026 A>G did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr23:26212769 C>T did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:26212412 A>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:140995732 A>G did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:140995702 C>G did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:140995781 G>T did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:140995581 C>T did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:140995590 C>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:140994859 A>G did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:140994994 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:140994571 G>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:140995923 G>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:140995191 G>A did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:140996142 G>C did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:140996153 G>C did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:140995352 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:140995432 C>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:140994933 C>G did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:140995306 C>G did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:140996084 G>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:140994849 C>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:140996227 A>G did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:140996560 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:140993420 G>C did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:141291532 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:141291505 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:141291462 C>G did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:141290678 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:141291216 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:141291552 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:141291580 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:140985240 A>C did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:140985526 G>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:140969320 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:140967083 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:140985490 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:140985256 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:140983081 G>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:140926177 G>A did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:140953295 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:140969302 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:140985491 C>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:140985614 G>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:51640677 G>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:51638458 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:51644850 G>C did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:54836516 A>C did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:54841171 G>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:54838616 G>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:54837355 G>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:75649157 G>T did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:75649173 T>C did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:75650842 G>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:75650227 G>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:75648894 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:75650024 C>T did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr23:75649242 C>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:75650412 G>T did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:75650396 G>T did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:75649296 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:75650538 C>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:75004087 G>C did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:75003365 C>A did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:75004381 C>G did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr23:75004434 G>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:75003989 C>A did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr3:184429383 G>A maps to NM_022149.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:55479402 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:55479402 C>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:23890378 G>A maps to NM_019066.4 V837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:23890783 T>A maps to NM_019066.4 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:23889232 C>G maps to NM_019066.4 A1219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr15:23890132 C>G maps to NM_019066.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr3:65425632 C>T maps to NM_001033057.1 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:77764506 G>A maps to NM_012301.3 I954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr7:77975257 C>T maps to NM_012301.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:78150945 G>T maps to NM_012301.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:78150906 A>G maps to NM_012301.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:78636447 G>A maps to NM_012301.3 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:49021257 A>T did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr23:77112281 C>G did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr23:77150832 G>C did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:77150847 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:95713852 G>A maps to NM_002371.2 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr18:56348414 G>T maps to NM_006785.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr9:72741226 C>A maps to NM_153267.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr9:139748259 T>C maps to ENST00000392881 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:95825559 C>A maps to NM_032427.1 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr11:95712800 C>A maps to NM_032427.1 G928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:149639718 A>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:149638333 T>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:149638837 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:118035834 C>G maps to NM_006699.3 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr9:140002865 C>T maps to NM_016219.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:26104630 G>A maps to NM_020379.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr5:109106206 C>T maps to NM_002372.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:91450581 C>T maps to NM_006122.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr15:91452554 A>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:12768922 C>G maps to NM_000528.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr19:12768934 C>A maps to NM_000528.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:75655060 C>G maps to NM_006715.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr15:75649168 G>A maps to NM_006715.2 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:96053794 C>T maps to NM_024641.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:96054244 A>G maps to NM_024641.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:12483225 G>C maps to NM_018050.2 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:43702930 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:43817846 G>A maps to ENST00000382031 E1630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr15:43819244 C>T maps to ENST00000382031 S2096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr15:43822397 C>T maps to ENST00000382031 F3034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:71495082 C>T maps to NM_005909.3 P1967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr5:71491800 C>A maps to NM_005909.3 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr5:71490072 C>G maps to NM_005909.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr5:71493129 G>A maps to NM_005909.3 K1316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:71489754 T>C maps to NM_005909.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr2:172944925 C>T maps to NM_199227.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:242161835 G>T maps to NM_001004343.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr1:242159551 G>A maps to NM_001004343.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr2:210560607 G>A maps to NM_002374.3 E1238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:210559380 C>T maps to NM_002374.3 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:210559533 A>G maps to NM_002374.3 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr2:210561311 A>G maps to NM_002374.3 K1409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr15:66727502 G>A maps to NM_002755.3 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr19:4099226 C>A maps to NM_030662.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:21208394 G>A maps to NM_145109.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr17:21204286 C>G maps to NM_145109.2 Y127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:21205555 G>A maps to NM_145109.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr17:21204223 G>A maps to NM_145109.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr17:12044543 A>T maps to ENST00000415385 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr15:67950888 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:67515455 G>T maps to NM_002758.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr17:67515557 C>T maps to NM_002758.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr5:56177954 C>T maps to NM_005921.1 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr5:56161202 C>T maps to NM_005921.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:65375869 C>T maps to NM_002419.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:53879204 C>T maps to NM_001193511.1 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:53881049 C>T maps to NM_001193511.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr12:53877248 C>G maps to NM_001193511.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr3:185181424 C>A maps to NM_004721.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:185184730 A>G maps to NM_004721.3 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:185146680 G>T maps to NM_004721.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr17:43350975 T>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:19389642 G>T did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:19387264 C>T did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:19398258 C>T did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:19380916 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:19398284 T>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:161470959 T>C maps to NM_005922.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr6:161510412 T>G maps to NM_005922.2 A961A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:161470014 A>T maps to NM_005922.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:136888769 T>A maps to NM_005923.3 R1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr6:136923060 C>T maps to NM_005923.3 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr6:136990472 G>C maps to NM_005923.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:136904833 G>C maps to NM_005923.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:27682927 C>T maps to NM_004672.3 Q1196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr14:71197216 C>T maps to NM_033141.2 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr14:71199922 G>T maps to NM_033141.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr19:39090610 C>G maps to NM_001042600.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr19:39090743 C>G maps to NM_001042600.1 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:39088219 G>A maps to NM_001042600.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:39086130 C>T maps to NM_001042600.1 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:39100634 G>T maps to NM_001042600.1 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:39090568 G>T maps to NM_001042600.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:64557881 G>A maps to NM_004579.2 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr2:39485728 C>T did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr2:102460736 T>A maps to NM_145686.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:102456380 C>T maps to NM_145686.2 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:102314985 G>T maps to NM_145686.2 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:102460598 C>T maps to NM_145686.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr2:102481429 C>G maps to NM_145686.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:75298964 C>T maps to NM_033063.1 K527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:75298589 G>T maps to NM_033063.1 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr23:20030524 C>T did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:20033399 G>A did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:20030580 T>C did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:20034288 G>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:135312595 A>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:135302934 T>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:135309468 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:135309465 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:135313039 G>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:135326827 G>T did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr23:135303014 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:135312672 T>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr22:22160159 G>T maps to NM_138957.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr22:50704661 G>C maps to NM_002751.5 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr22:50694043 C>T maps to NM_002969.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr8:144803247 G>A maps to NM_139021.2 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr8:144803719 G>A maps to NM_139021.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr14:55529997 G>A maps to NM_144578.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:48241501 C>T maps to NM_002747.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr18:48255611 G>T maps to NM_002747.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr15:52353665 G>T maps to NM_002748.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:19284862 C>T maps to NM_139034.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:45923587 C>A maps to NM_005456.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr22:51040244 A>G maps to ENST00000329492 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:1756651 G>A maps to NM_015133.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr3:50679720 C>T maps to NM_004635.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:50677814 A>T maps to NM_004635.3 K80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:112318305 C>A maps to NM_139078.1 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr15:42109933 G>T did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr15:42106795 C>T maps to NM_001128608.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr18:32677485 G>A maps to NM_014268.2 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:27245130 G>T maps to NM_012326.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:164506933 G>A maps to ENST00000514618 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:60813356 G>A maps to NM_152598.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr17:60865909 G>C maps to NM_152598.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:16177919 C>T maps to NM_001102562.1 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:16090996 C>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:8491528 G>T maps to NM_016496.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr19:8503279 C>T maps to NM_016496.4 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:94109447 C>A maps to NM_017824.4 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:10426587 C>T maps to NM_005885.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:10405728 A>T maps to NM_005885.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:10405768 C>T maps to NM_005885.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:10402205 C>T maps to NM_005885.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:10417440 G>C maps to NM_005885.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr5:10402649 T>C maps to NM_005885.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:10414597 C>T maps to NM_005885.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:10390500 T>C maps to NM_005885.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:10382033 G>T maps to NM_005885.2 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr10:45953835 C>A maps to NM_145021.4 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:119750053 T>C did not map to a codon.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:119739939 C>A maps to NM_006770.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr2:119732097 C>T maps to NM_006770.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:119699911 C>G maps to NM_006770.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:220809368 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:220835152 G>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr14:103915264 G>T maps to ENST00000335102 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:103931943 C>T maps to ENST00000335102 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr14:103946809 G>A maps to ENST00000335102 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:45803084 G>C maps to NM_031417.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:57910228 C>T maps to NM_004990.2 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:57884122 C>G maps to NM_004990.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:198570719 C>T maps to NM_138395.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:198570869 C>T maps to NM_138395.3 D247D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-3406-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:71674662 C>G maps to NM_001017967.2 L322L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-66-2766-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:71663315 C>A maps to NM_001017967.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:160328350 C>T maps to NM_002377.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr6:29455058 T>C maps to NM_052967.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:186980424 G>A maps to NM_139125.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr3:186937969 C>T maps to NM_001879.5 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:186980460 G>T maps to NM_139125.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:186959293 C>A maps to NM_139125.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:12969500 C>T maps to NM_014975.2 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:12963059 A>T maps to NM_014975.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:46290250 G>T maps to NM_015112.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:18233560 G>A maps to NM_015016.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:66396420 G>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:66460892 C>A maps to NM_001164664.1 S1962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:66461702 C>T maps to NM_001164664.1 L2232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:66427716 G>T maps to NM_001164664.1 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr10:82034379 C>T maps to NM_000429.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:3783853 G>A maps to NM_002378.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:98943538 C>T maps to ENST00000254898 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:43932921 C>A maps to ENST00000372754 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:138654710 A>T maps to ENST00000394800 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr16:29819135 A>T maps to NM_001042539.1 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr16:29818991 C>T maps to NM_001042539.1 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr22:36003351 G>A maps to NM_203377.1 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr18:47799295 C>T maps to ENST00000424334 K589K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:149243367 C>A maps to ENST00000404807 S1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr12:57921291 C>T maps to NM_052897.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr10:54531334 C>A maps to NM_000242.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:131526208 C>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:54687470 C>T maps to NM_024298.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr16:84094377 C>T maps to NM_003791.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:21896173 G>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:21896717 C>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr23:21900555 T>C did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr18:13884818 G>T maps to NM_000529.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:58038583 T>C maps to NM_005912.2 *333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:58039352 G>T maps to NM_005912.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr18:13826054 C>T maps to NM_005913.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:112487111 G>T maps to NM_001085377.1 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:182733348 G>T maps to NM_020166.3 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:138699717 C>T did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:138714594 A>G did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:138714569 G>C did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:138711967 C>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:138670584 C>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:138671993 C>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:138713647 C>A did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:138699859 G>T did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr23:138680614 A>G did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:138708791 T>C did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:138692463 A>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:138679675 C>G did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:138679722 C>A did not map to a codon.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr23:138687051 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:182947452 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr3:182933803 T>A maps to NM_015078.2 K817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:183035888 G>C maps to NM_015078.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr3:183041139 C>A did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr3:183014823 C>T maps to NM_015078.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:41077493 C>T maps to NM_005297.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr22:41077844 G>T maps to NM_005297.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr22:41077400 T>G maps to NM_005297.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:100390822 A>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:100368896 C>T maps to NM_032503.2 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:100403964 C>T maps to NM_032503.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:150550761 G>T maps to NM_021960.4 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr10:13222486 C>A maps to NM_182751.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr10:13214718 A>G maps to NM_182751.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:127327757 A>G maps to NM_004526.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:127323595 C>T maps to NM_004526.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr3:127335786 C>G maps to NM_004526.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:127327751 C>T maps to NM_004526.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:127335942 C>T maps to NM_004526.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr6:52131487 C>T maps to ENST00000419835 K738K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr6:52143601 G>A maps to ENST00000419835 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:47663397 G>A maps to NM_003906.3 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr21:47676827 G>T maps to NM_003906.3 C1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr22:35799326 G>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:136617012 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr2:136620286 C>A maps to NM_005915.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:5966672 C>T maps to NM_032485.4 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr20:5965432 G>T maps to NM_032485.4 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:6289032 G>T maps to NM_024596.3 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:49958313 C>A maps to NM_001012300.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:119742190 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:30672561 G>C maps to NM_014641.2 T1466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr6:30672864 T>C maps to NM_014641.2 S1365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:30673548 G>C maps to NM_014641.2 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr6:30668370 A>C maps to NM_014641.2 P2047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr6:30671676 C>T maps to NM_014641.2 V1761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:37611678 C>A maps to ENST00000297153 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr6:37605155 C>T maps to ENST00000297153 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr6:37614073 C>T maps to ENST00000297153 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:47504453 C>A maps to NM_001113498.2 G527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr14:47351271 T>C maps to NM_001113498.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:47426787 G>T maps to NM_001113498.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr14:47351379 C>T maps to NM_001113498.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr14:47389250 C>T maps to NM_001113498.2 V734V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr14:47504429 G>A maps to NM_001113498.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr2:63834096 T>A maps to NM_005917.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:207625737 C>A did not map to a codon.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr7:75689710 C>A maps to NM_005918.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr12:68707530 G>C maps to NM_017440.4 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:68716990 T>A maps to NM_017440.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:204507404 C>A maps to NM_002393.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:90499891 G>A maps to NM_014611.1 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:90387320 G>T maps to NM_014611.1 S4169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:90435039 C>A maps to NM_014611.1 E1850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr6:90354760 A>G maps to NM_014611.1 F5525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr6:90460070 A>G did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:90450018 C>T maps to NM_014611.1 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:90497610 C>T maps to NM_014611.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:90472116 T>C maps to NM_014611.1 K759K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:90482390 G>A maps to NM_014611.1 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr6:90460226 T>A maps to NM_014611.1 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr6:90499527 C>A maps to NM_014611.1 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr6:90382275 T>C maps to NM_014611.1 Q4540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr6:90415837 T>A maps to NM_014611.1 A2696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr6:84055987 G>A maps to NM_002395.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:84108235 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr18:48434456 C>T maps to NM_002396.4 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr18:48450550 A>G maps to NM_002396.4 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr11:86209148 A>G maps to NM_001014811.1 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:168825716 A>G maps to NM_004991.3 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:168830640 A>G maps to NM_004991.3 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:153295969 G>C did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:153296298 G>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:153297675 T>C did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:37563745 C>A maps to NM_004774.3 V1576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr17:37565860 G>A maps to NM_004774.3 N871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:37571340 G>T maps to NM_004774.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:70347885 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:70343464 G>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:70349257 C>G did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:70351453 A>C did not map to a codon.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr23:70349705 G>A did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr3:151112453 A>G maps to NM_053002.4 R1838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr3:151085965 G>T maps to NM_053002.4 G1124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:150908644 C>A maps to NM_053002.4 S632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:150834174 C>A maps to NM_053002.4 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr3:151067920 A>G maps to NM_053002.4 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr12:116675333 T>C maps to NM_015335.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:116549242 G>A maps to NM_015335.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:116424271 C>T maps to NM_015335.4 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:116429527 G>A maps to NM_015335.4 T1077T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:40534579 C>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:40513613 A>T did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr23:40551536 C>T did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:40539209 C>T did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:40562732 T>C did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr22:20939444 C>T maps to NM_001003891.1 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr19:872082 C>A maps to NM_005481.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:875361 G>C maps to NM_005481.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr6:131946126 C>T maps to ENST00000403834 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr17:38192030 C>T maps to NM_014815.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:38183200 G>A maps to NM_014815.3 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:38209751 C>A maps to NM_014815.3 G34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:134814845 C>T maps to NM_004269.2 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr9:134955030 G>C maps to NM_004269.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:17623208 G>T did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr4:17616309 G>T maps to NM_025205.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr8:118533159 C>G maps to NM_080651.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:118533153 C>T maps to NM_080651.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:71063402 C>A maps to ENST00000430055 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:88047821 G>A maps to NM_002397.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:156450723 C>A maps to NM_005920.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:156452387 A>G maps to NM_005920.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:3304209 C>A maps to NM_000243.2 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr5:126755733 A>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:66223227 C>A maps to NM_032445.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:3512011 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr19:42863287 G>T maps to ENST00000251268 G1794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:42860340 C>G maps to ENST00000251268 S1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr22:42099441 C>T maps to NM_152513.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr22:42172158 G>A maps to NM_152513.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:47912412 C>T maps to NM_020160.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr19:47912499 G>A maps to NM_020160.1 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:36665427 T>C maps to NM_014791.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:32145974 T>A maps to NM_015955.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:32145918 G>A maps to NM_015955.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:46801050 C>A maps to NM_005588.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:46777262 A>G maps to NM_005588.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:46800902 C>T maps to NM_005588.2 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr6:46803247 C>T maps to NM_005588.2 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:100029209 C>T maps to NM_019606.5 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:100028426 G>A maps to NM_019606.5 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr4:88766126 A>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr4:88766514 G>T maps to ENST00000395102 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:112755044 A>C maps to NM_006343.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:116415133 G>C maps to NM_001127500.1 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr7:116411550 G>C did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:116340286 G>T maps to NM_001127500.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:116380910 G>T maps to NM_001127500.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr17:81043113 G>A maps to NM_001004431.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr14:21458711 C>T maps to NM_001029991.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:171755079 G>C maps to NM_015935.4 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:171755046 C>G maps to NM_015935.4 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:171765853 G>T maps to NM_015935.4 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:171765715 G>T maps to NM_015935.4 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:128141837 C>A maps to NM_018396.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr14:21968794 G>A maps to NM_019852.3 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr3:15466467 A>T maps to NM_152396.2 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:172195692 C>G did not map to a codon.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr1:156047122 C>A maps to NM_001093725.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr18:48702951 A>G maps to NM_016626.4 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr18:48703428 C>A maps to NM_016626.4 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:196733570 G>C maps to NM_005929.5 S596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:179069769 C>T maps to NM_033540.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:179096196 C>T maps to NM_033540.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:179096547 G>A maps to NM_033540.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:179096535 A>G maps to NM_033540.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr3:179069751 A>T maps to NM_033540.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr22:37882167 G>C maps to NM_002405.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr3:158539384 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:158541979 C>A maps to NM_022736.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr12:53646885 C>A maps to NM_001170790.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:191353381 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:191301380 C>A maps to NM_017694.3 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr17:8701181 C>A maps to NM_152599.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:678525 G>A maps to ENST00000404286 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr4:128851935 C>T maps to NM_152778.2 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr15:42057171 A>G maps to ENST00000219905 L2660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:42003148 C>A maps to ENST00000219905 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:141754597 G>C maps to ENST00000475668 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:141740547 A>G maps to ENST00000475668 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:141736021 G>A maps to ENST00000475668 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr7:141758050 C>T maps to ENST00000475668 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:141800655 G>A maps to ENST00000475668 G2644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr7:141765164 G>T maps to ENST00000475668 G1505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:141752639 C>T maps to ENST00000475668 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:141722155 G>T maps to ENST00000475668 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:180219176 A>T maps to NM_001114617.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr14:50088625 G>T maps to NM_002408.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr22:39884665 C>T maps to NM_001098270.1 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr22:39883957 G>A maps to NM_001098270.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr22:39884065 C>A maps to NM_001098270.1 C238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr12:86373489 A>T maps to ENST00000393205 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:135012093 T>G maps to NM_002410.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:74928784 G>A maps to NM_198955.1 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:74944913 T>C maps to NM_198955.1 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr7:88423637 G>A maps to NM_152706.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:43280395 G>A maps to NM_153361.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:103550820 G>A maps to NM_012215.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:103559212 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:39722272 A>T did not map to a codon.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:222835655 G>A maps to NM_198551.2 R1748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:222791475 C>T maps to NM_198551.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:222828094 C>T maps to NM_198551.2 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:222806449 A>T maps to NM_198551.2 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:222833077 C>A maps to NM_198551.2 L1603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:222801476 G>A maps to NM_198551.2 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr18:19379820 G>A maps to NM_020774.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:1562239 G>T maps to NM_080875.2 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:109766433 G>A maps to NM_022765.3 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:12280013 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:18387539 G>A maps to NM_015241.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr22:18301124 G>A maps to NM_015241.2 S1434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr22:18300434 C>T maps to NM_015241.2 K1664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr22:18374398 C>G did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:12315631 T>A maps to NM_032867.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:38320667 G>A maps to NM_033386.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:1489874 C>A did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr7:1487279 T>C maps to NM_182924.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:31475279 G>A maps to NM_005931.3 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:10450577 A>T did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr23:10535111 T>C did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:107169339 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:107160756 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:1255490 C>T maps to NM_177401.4 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:67411869 A>T maps to NM_001077700.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:97677933 C>T maps to NM_153182.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:97677948 G>C maps to NM_153182.2 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:97664060 G>T maps to NM_153182.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr7:7636040 C>A maps to NM_019005.3 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:7645636 C>T maps to NM_019005.3 N822N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr7:7612492 A>T maps to NM_019005.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:7628157 A>G maps to NM_019005.3 R616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr12:56845174 G>T maps to NM_012064.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr13:24443476 G>T maps to NM_005932.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:37739623 G>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:37717106 C>G maps to NM_001195296.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:37969325 C>A maps to NM_001195296.1 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:70008495 G>A maps to ENST00000448226 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:129903800 T>A maps to NM_002417.4 I2101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:129903463 C>A maps to NM_002417.4 E2214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr22:40816852 T>C maps to NM_020831.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr22:40825652 C>T maps to NM_020831.3 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr16:14340859 C>T maps to NM_014048.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr7:131099444 C>T maps to NM_013255.4 Q275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:2043171 G>A maps to NM_199054.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr15:23811399 G>C maps to NM_005664.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr15:23812393 G>T maps to NM_005664.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr15:23811489 A>C maps to NM_005664.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:23811258 G>A maps to NM_005664.3 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr15:23812323 T>G maps to NM_005664.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:23811408 C>A maps to NM_005664.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr15:23811259 G>T maps to NM_005664.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr15:23811654 G>T maps to NM_005664.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr17:56291732 G>C maps to NM_017777.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:56293531 G>A maps to NM_017777.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr10:28032254 G>C maps to NM_173576.2 Y30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:121134305 C>T maps to NM_014730.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:158317861 T>A maps to NM_001195432.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr3:158317958 G>T maps to NM_001195432.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr12:6859056 C>A maps to NM_005439.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:37061818 G>A maps to NM_000249.3 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:37061852 G>T maps to NM_000249.3 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr14:75514842 C>A maps to NM_001040108.1 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:75513082 C>T maps to NM_001040108.1 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr16:74725173 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:118376854 G>A maps to NM_001197104.1 Q3416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:118344237 C>A maps to NM_001197104.1 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:118376002 C>G maps to NM_001197104.1 L3132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr11:118352800 G>T maps to NM_001197104.1 E1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:118374739 G>A maps to NM_001197104.1 Q2711Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:118372450 T>A maps to NM_001197104.1 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:49442949 C>A maps to NM_003482.3 G1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr12:49427254 G>A maps to NM_003482.3 Q3745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:49431141 G>A maps to NM_003482.3 Q3333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:49434375 C>A maps to NM_003482.3 E2393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr12:49443463 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:49431526 T>A maps to NM_003482.3 P3204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:49416381 G>T maps to NM_003482.3 Y5443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:49443898 C>A maps to NM_003482.3 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr12:49420840 C>A maps to NM_003482.3 E4970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:49435056 G>A maps to NM_003482.3 Q2166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr12:49421038 G>A maps to NM_003482.3 R4904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:49444669 T>A maps to NM_003482.3 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr12:49446493 T>A did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr12:49437449 G>C maps to NM_003482.3 S1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:49445463 C>A maps to NM_003482.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr12:49431060 G>A maps to NM_003482.3 Q3360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:49448309 C>T did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr12:49421837 G>A maps to NM_003482.3 P4823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr12:49445908 G>A maps to NM_003482.3 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr12:49444813 A>G maps to NM_003482.3 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr7:152009026 G>A maps to ENST00000355193 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:151880069 T>A maps to ENST00000355193 K1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr7:151932934 C>T maps to ENST00000355193 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:151879573 G>A maps to ENST00000355193 Q1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:151874730 T>A maps to ENST00000355193 R2603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:151878025 T>A maps to ENST00000355193 R2307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr7:151879118 T>C maps to ENST00000355193 T1942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:152055755 G>A maps to ENST00000355193 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr7:151874634 G>A maps to ENST00000355193 Q2635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:151970856 G>A maps to ENST00000355193 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:151962223 A>T maps to ENST00000355193 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:151851427 C>A maps to ENST00000355193 L4078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:151962220 A>T maps to ENST00000355193 C362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:36218349 G>T maps to NM_014727.1 E1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:36218435 G>C maps to NM_014727.1 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:36223338 G>A maps to NM_014727.1 P1963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:36227819 G>A maps to NM_014727.1 W2435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:104742346 A>G maps to NM_182931.2 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr7:104702724 G>T maps to NM_182931.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr10:22021981 G>C maps to NM_004641.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr10:22002758 A>G maps to NM_004641.3 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr10:21959403 T>A maps to NM_004641.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:22002879 G>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr10:21959504 C>G maps to NM_004641.3 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:151039901 G>T maps to NM_006818.3 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr9:20414000 A>C maps to NM_004529.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:168352698 C>T maps to ENST00000400822 D1547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:168352585 C>T maps to ENST00000400822 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr6:168317905 C>T maps to ENST00000400822 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:33768841 G>A maps to NM_002418.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:238461035 A>T maps to NM_024101.5 R578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr2:238443204 A>C did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr2:238419718 C>A maps to NM_024101.5 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr16:2256501 C>T maps to NM_022372.4 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:122619801 C>T maps to NM_014938.3 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr7:73021341 T>A maps to NM_032951.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:109998842 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:154878199 A>G maps to NM_007289.2 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr3:154857993 T>C maps to NM_007289.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:154866430 G>T maps to NM_007289.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr3:154834693 G>A maps to NM_007289.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:154884811 T>A did not map to a codon.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:154862191 T>C maps to NM_007289.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:154832873 C>G maps to NM_007289.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:2527474 C>T maps to NM_033467.3 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:102661199 C>T maps to NM_002421.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:102667841 A>T maps to NM_002421.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr22:24121531 G>C maps to NM_005940.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:102745646 C>A maps to ENST00000326227 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr16:58077460 C>T maps to NM_002428.2 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr8:89179935 G>T maps to NM_005941.4 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:89053689 C>T maps to NM_005941.4 *608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:89339429 G>T maps to NM_005941.4 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:89128774 G>A maps to NM_005941.4 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:89128849 T>A maps to NM_005941.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr8:89198753 G>A maps to NM_005941.4 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr8:89130995 G>T maps to NM_005941.4 Y268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr12:56232465 G>T maps to NM_002429.4 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:56231416 G>C maps to NM_002429.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr16:55523689 A>T maps to NM_004530.4 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr16:55516924 A>C maps to NM_004530.4 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:102479830 T>C did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:127464381 G>A maps to NM_147191.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:127464270 T>C maps to NM_147191.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:3107200 C>T maps to NM_022468.4 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:5013284 T>A maps to NM_021801.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:5012676 T>A maps to NM_021801.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:34095372 G>A maps to NM_024302.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr17:34100370 C>A maps to NM_024302.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:34095264 G>A maps to NM_024302.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:102713524 C>A maps to NM_002422.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:102398591 G>T maps to NM_002423.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:102595562 T>C maps to NM_002424.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr11:102586032 A>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:102592221 C>A maps to NM_002424.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:44642295 G>T maps to NM_004994.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:90857905 G>C maps to NM_007351.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:90830529 G>T maps to NM_007351.2 G243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr10:88703343 C>T maps to NM_024756.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr10:88703037 C>A maps to NM_024756.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr10:88702233 G>A maps to NM_024756.2 D769D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr10:99221791 G>A maps to ENST00000422291 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr22:28196345 G>A maps to NM_002430.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:158813150 C>A maps to NM_002432.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:156799190 G>C maps to NM_005515.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr14:93650149 C>T maps to NM_022151.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:2078283 C>T maps to NM_130807.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:198380839 G>C maps to NM_015387.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr18:33800109 G>A maps to NM_017947.2 Q630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr18:33775226 C>G maps to NM_017947.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr6:39881097 G>T maps to ENST00000425303 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:49576167 C>T maps to NM_014484.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:75438598 G>C maps to NM_025098.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:75438509 C>A maps to NM_025098.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:75442216 G>A maps to NM_025098.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:100842048 C>T maps to NM_178176.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:100841536 G>A maps to NM_178176.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr12:62954652 A>T maps to ENST00000393630 L1265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr12:62894644 A>T maps to ENST00000393630 A216A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-60-2698-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr12:62887714 G>T maps to ENST00000393630 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:62931380 G>T did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr3:108723687 A>G maps to NM_014429.3 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:108723702 C>T maps to NM_014429.3 W682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:108776293 T>A maps to NM_014429.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:108724126 G>A maps to NM_014429.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr3:108812287 C>T maps to NM_014429.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:108813789 C>T maps to NM_014429.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:108776333 C>T did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr22:31345807 G>A maps to ENST00000397641 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:106205334 G>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:106185170 T>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:106228350 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:106228455 C>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr15:79172852 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:102931461 C>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:102931101 C>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr23:102931644 C>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:102931867 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:122107251 C>T maps to NM_173855.4 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr9:124936895 A>T maps to NM_198469.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:57025719 G>A maps to NM_005372.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:57026205 C>A maps to NM_005372.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:134025617 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:14933877 C>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:14936841 C>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:100211220 C>T maps to NM_023948.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:100210479 G>T maps to NM_023948.4 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:113231655 C>A maps to NM_020963.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr22:50552828 C>T maps to NM_018995.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr22:50547271 C>T maps to NM_018995.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr6:132693968 G>A maps to NM_015529.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr6:132618997 G>C maps to NM_015529.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:7487218 C>A maps to NM_004870.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr9:13110739 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr9:13176149 G>T maps to ENST00000319217 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:58978322 G>A maps to NM_001039396.1 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:58979666 G>A maps to NM_001039396.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr11:58978895 G>A maps to NM_001039396.1 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr11:58978607 G>A maps to NM_001039396.1 C577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:58980282 G>C maps to NM_001039396.1 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:58978604 G>C maps to NM_001039396.1 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr13:20240599 C>A maps to ENST00000414242 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:123641362 T>C maps to NM_022782.2 A1029A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:123687513 G>A maps to NM_022782.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr15:75189481 C>A maps to NM_002435.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:43818204 C>G maps to NM_005373.2 S557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:43804365 G>A maps to NM_005373.2 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:4355106 C>G maps to ENST00000262967 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:56350925 G>A maps to ENST00000340482 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr17:56348127 G>A maps to ENST00000340482 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr17:56348154 G>T maps to ENST00000340482 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:154009997 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:41891577 C>A maps to ENST00000398393 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:41895441 C>T maps to ENST00000398393 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:202545688 T>C maps to NM_033066.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr14:67787834 G>A maps to NM_022474.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr14:67787013 G>A maps to NM_022474.2 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr10:28345546 C>T maps to NM_173496.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr10:28348634 A>T maps to NM_173496.3 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:30439181 T>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:30516882 C>A maps to NM_001584.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr22:37425398 C>A maps to NM_021126.4 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:27535959 C>A maps to ENST00000405983 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:18304773 A>G maps to NM_032683.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:167742572 T>C maps to NM_003953.5 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:181018380 G>T maps to NM_001531.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr21:33684246 C>T maps to ENST00000445271 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr21:33678948 A>G did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:84772675 G>T maps to NM_138409.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:138119440 C>A maps to NM_001085049.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr3:138091772 G>T maps to NM_001085049.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:60742269 C>A maps to NM_006039.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:60759626 C>A maps to NM_006039.3 A945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:94180421 C>T maps to NM_005591.3 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:68747786 G>A maps to NM_198923.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:68748107 C>T maps to NM_198923.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:68748335 G>A maps to NM_198923.2 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr11:3249738 G>C maps to ENST00000328215 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:68773486 C>A maps to NM_145015.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:68773710 C>A maps to NM_145015.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:18955914 T>C maps to NM_147199.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:18195696 G>A maps to NM_054032.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr11:18195312 T>C maps to NM_054032.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr11:18194895 G>A maps to NM_054032.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:79671381 C>T maps to NM_002949.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:59574275 G>T maps to NM_017840.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:160218357 T>C maps to NM_014161.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:75874309 C>T maps to NM_014763.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr5:154330395 A>T maps to NM_014180.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr7:42972005 C>G maps to NM_031903.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr7:42977162 C>T maps to NM_031903.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr2:224824685 C>T maps to NM_022915.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:36462505 G>A maps to NM_032351.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr3:179320568 A>G maps to NM_020409.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:6601441 G>A maps to NM_016497.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:228295502 G>A maps to NM_181462.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:151732534 G>C maps to NM_031420.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:36921955 C>T maps to NM_031280.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr7:56020980 C>A maps to ENST00000426595 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr6:30593546 G>A maps to NM_014046.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:139069034 C>A maps to NM_020191.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr7:43906543 C>A maps to NM_032014.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr5:71521967 C>T maps to ENST00000513900 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr8:80942389 C>A maps to NM_014018.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr5:44815183 T>C maps to NM_016640.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:44809297 G>A maps to NM_016640.3 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:44813254 C>T maps to NM_016640.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:95770427 C>A maps to NM_031902.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:125054074 G>C maps to NM_138777.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:10602077 C>A maps to NM_001098579.1 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr11:10622582 C>T maps to NM_001098579.1 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:60235939 A>T maps to NM_152866.2 *298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr11:60557883 C>T maps to NM_206893.3 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr11:60264961 G>A maps to NM_017716.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:60268609 C>A maps to NM_017716.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:60183134 G>T maps to NM_032597.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr11:60540958 T>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:59828659 A>T maps to NM_006138.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr11:60059778 A>T maps to NM_148975.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:60105242 G>C maps to NM_139249.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr11:60107343 T>A maps to NM_139249.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:60102449 G>T maps to NM_139249.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr11:60482866 G>T maps to NM_031457.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr11:60482588 C>A maps to NM_031457.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:60470903 G>C maps to NM_031457.1 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:72755879 C>T maps to NM_005098.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:17998201 C>A maps to NM_001105569.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr5:80074604 C>G maps to NM_002439.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:79968170 G>T maps to NM_002439.3 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr5:79950592 C>A maps to NM_002439.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:80063921 C>A maps to NM_002439.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:76343989 A>G maps to NM_002440.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:76280710 T>C maps to NM_002440.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:76363641 C>T maps to NM_002440.2 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:31725964 G>A maps to ENST00000375742 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:48026132 G>A maps to NM_000179.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:48018262 G>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr12:120789150 A>G maps to NM_002442.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:11783733 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:11780325 G>C did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:11786712 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:818699 C>T maps to NM_013404.4 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr16:830136 G>C maps to NM_001025190.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr16:819470 A>C maps to NM_001025190.1 L1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr16:823223 G>A maps to NM_001025190.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr10:51562372 C>A maps to NM_002443.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:35753242 C>A maps to NM_001044264.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:64951019 G>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:64959615 C>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:64949368 G>C did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:64956698 G>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:64957194 C>G did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr8:15978097 G>T maps to ENST00000445506 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr8:16001065 C>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr8:16026113 G>T maps to ENST00000445506 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:49723333 G>A maps to NM_020998.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:131188763 G>A did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:131206863 G>C did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:131206390 T>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:190922313 C>T maps to NM_005259.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:190924988 G>A maps to NM_005259.2 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr4:4864839 T>C maps to NM_002448.3 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr16:56673831 G>C maps to NM_005946.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:105905015 C>G maps to NM_004689.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:62361825 C>G maps to NM_004739.2 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr2:42871301 A>G maps to ENST00000405094 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:42936084 A>G maps to ENST00000405094 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr2:42871289 C>G maps to ENST00000405094 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr8:121509645 G>A maps to NM_022045.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr8:121514774 C>A maps to NM_022045.3 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:47660337 G>A maps to NM_014342.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:154294058 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr8:97269294 C>A maps to NM_015942.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr8:97263323 C>G did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:242035675 T>A maps to NM_182501.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:38323189 G>T maps to NM_005955.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr10:135233566 A>T maps to NM_138384.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:64898344 C>T maps to NM_005956.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr16:86565979 C>T maps to NM_001159377.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:55490958 T>A maps to NM_002453.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr13:28011399 C>G maps to NM_152912.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:149814184 G>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:149895708 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:149902773 G>A maps to NM_001145862.1 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:149906926 C>A maps to NM_001145862.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:32274180 C>A maps to NM_001040446.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr5:32239229 C>T maps to NM_001040446.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:9739393 G>A did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr22:30415745 G>T maps to NM_021090.3 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:30416604 C>G maps to NM_021090.3 S986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr17:56569100 C>A maps to NM_004687.4 E1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:25831402 C>T maps to NM_004685.3 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:63488507 G>T did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:63548672 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:63488711 T>C did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr23:63568543 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:11167122 G>A maps to NM_015458.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr1:11259717 C>G maps to NM_004958.3 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:11297935 G>A maps to NM_004958.3 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:11307699 G>A maps to NM_004958.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:11217270 G>T maps to NM_004958.3 T1469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:30625752 G>T maps to ENST00000358107 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:237016388 G>A did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:236998968 C>T maps to NM_000254.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:236976068 G>A maps to NM_000254.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr13:41834926 C>A maps to NM_004294.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:41826880 G>A maps to NM_004294.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:153311083 C>T maps to NM_019041.5 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr8:125565385 G>T maps to NM_014751.4 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr4:100504544 T>C maps to ENST00000511045 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:100518256 C>T maps to ENST00000511045 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:100510801 C>G maps to ENST00000511045 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:100515904 G>C maps to ENST00000511045 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:100503107 C>G maps to ENST00000511045 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr8:17512164 A>C maps to NM_001001924.2 L1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr8:17611495 G>C maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr8:17611495 G>C maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:29599056 C>T maps to NM_001033602.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr13:29600301 T>C maps to NM_001033602.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr13:29608119 C>A maps to NM_001033602.2 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr13:29608251 C>A maps to NM_001033602.2 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr13:29599635 G>A maps to NM_001033602.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr13:29855874 G>A maps to NM_001033602.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr13:29599083 C>A maps to NM_001033602.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr13:29600145 G>T maps to NM_001033602.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:155162051 T>A maps to ENST00000425082 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:124632523 G>A maps to NM_033049.3 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:26584732 G>A maps to NM_001135091.1 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:9056520 C>A maps to NM_024690.2 E10309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:8969304 G>A maps to NM_024690.2 Q14347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:8997447 C>T maps to NM_024690.2 R13658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:9013860 G>A maps to NM_024690.2 S12843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:9060340 G>A maps to NM_024690.2 S9035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:9061306 G>A maps to NM_024690.2 I8713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:9065830 T>A maps to NM_024690.2 T7205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:9071158 A>T maps to NM_024690.2 T5429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:9072085 A>G maps to NM_024690.2 S5120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:9061577 G>T maps to NM_024690.2 S8623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr19:9057325 C>T maps to NM_024690.2 P10040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:9000453 G>T maps to NM_024690.2 V13510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr19:9045651 G>T maps to NM_024690.2 T11993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr19:9019621 C>T maps to NM_024690.2 R12508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr19:9057250 G>A maps to NM_024690.2 S10065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:9058344 C>A maps to NM_024690.2 E9701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:9056896 T>A maps to NM_024690.2 P10183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr19:9067240 G>A maps to NM_024690.2 I6735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:9087692 G>T maps to NM_024690.2 P1374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:9005595 T>C maps to NM_024690.2 G13270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:9020772 G>A maps to NM_024690.2 T12443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:9058507 G>C maps to NM_024690.2 T9646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:8976593 G>A maps to NM_024690.2 L14128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:9020766 G>A maps to NM_024690.2 L12445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:9056707 G>A maps to NM_024690.2 F10246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:9070864 G>A maps to NM_024690.2 S5527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:9062191 C>T maps to NM_024690.2 L8418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:9060166 G>A maps to NM_024690.2 T9093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:9063784 G>A maps to NM_024690.2 T7887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr19:9072934 G>T maps to NM_024690.2 T4837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr19:9065821 G>T maps to NM_024690.2 A7208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr19:9003658 G>T maps to NM_024690.2 L13327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr19:9063187 T>A maps to NM_024690.2 P8086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:9075134 G>C maps to NM_024690.2 S4104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr19:9058960 G>A maps to NM_024690.2 T9495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr19:8993439 G>A maps to NM_024690.2 S13883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:9070726 C>T maps to NM_024690.2 G5573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:9090236 C>T maps to NM_024690.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:9010657 G>A maps to NM_024690.2 P13001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:9024994 G>C maps to NM_024690.2 P12289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:9089942 G>T maps to NM_024690.2 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:9017355 G>C maps to NM_024690.2 L12656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr19:9038136 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:9033666 G>A maps to NM_024690.2 D12090D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:9083648 G>T maps to NM_024690.2 L2722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:9089840 C>A maps to NM_024690.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr19:9046737 C>A maps to NM_024690.2 V11631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:8996330 G>C maps to NM_024690.2 L13747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:9026255 C>A maps to NM_024690.2 E12244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:9072229 G>C maps to NM_024690.2 L5072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr19:9058438 A>C maps to NM_024690.2 S9669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr19:9067654 C>A maps to NM_024690.2 V6597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:9068662 C>T maps to NM_024690.2 K6261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:9058096 A>T maps to NM_024690.2 S9783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:8994500 G>A maps to NM_024690.2 F13797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr19:9057421 T>C maps to NM_024690.2 S10008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr19:9066586 C>A maps to NM_024690.2 L6953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr19:9087485 C>A maps to NM_024690.2 L1443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:9009680 G>C maps to NM_024690.2 L13015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr19:9056704 T>A maps to NM_024690.2 P10247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9002183 G>A maps to NM_024690.2 F13440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9009661 G>A maps to NM_024690.2 L13022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9048214 G>C maps to NM_024690.2 S11139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9086273 G>T maps to NM_024690.2 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9087315 G>C maps to NM_024690.2 S1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9088080 G>C maps to NM_024690.2 S1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9089022 G>C maps to NM_024690.2 S931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9089300 G>C maps to NM_024690.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr19:9077424 C>A maps to NM_024690.2 G3341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr7:100683975 C>A maps to NM_001040105.1 T3093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr7:100683042 C>A maps to NM_001040105.1 V2782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:100676742 T>G maps to NM_001040105.1 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr7:100679805 C>A maps to NM_001040105.1 A1703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:100682799 C>G maps to NM_001040105.1 T2701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:100677336 T>G maps to NM_001040105.1 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:100682916 C>T maps to NM_001040105.1 S2740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:100684578 C>G maps to NM_001040105.1 A3294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:100678115 C>G maps to NM_001040105.1 S1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:100678752 T>C maps to NM_001040105.1 S1352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:100679391 C>A maps to NM_001040105.1 T1565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr7:100675755 A>G maps to NM_001040105.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr7:100676941 T>C maps to NM_001040105.1 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr7:100678758 C>T maps to NM_001040105.1 I1354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr7:100696356 G>T maps to NM_001040105.1 G4398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:100682142 C>T maps to NM_001040105.1 D2482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:100677407 C>A maps to NM_001040105.1 S904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr7:100675506 T>A maps to NM_001040105.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:100677873 G>T maps to NM_001040105.1 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:1098685 C>T maps to ENST00000441003 Y2352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:1085940 G>A maps to ENST00000441003 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:1087494 T>A maps to ENST00000441003 C1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:1093583 A>T maps to ENST00000441003 A1801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:1097312 C>T maps to ENST00000441003 F2243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr3:195452919 C>A maps to ENST00000447234 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr6:30955949 C>T maps to NM_001010909.2 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:195480066 G>T maps to NM_018406.5 S5121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:195487764 G>A maps to NM_018406.5 N4946N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:195474070 C>A maps to NM_018406.5 L5405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr3:195477898 G>C maps to NM_018406.5 V5244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:195481243 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr3:195486097 C>T maps to NM_018406.5 V4961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:1266002 A>T maps to ENST00000447027 P2634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:1271669 C>A maps to ENST00000447027 T4523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr11:1267379 C>A maps to ENST00000447027 T3093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr11:1253772 C>A maps to ENST00000447027 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr11:1261411 C>A maps to ENST00000447027 C1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr11:1281020 T>A maps to ENST00000447027 C5586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:1263974 C>T maps to ENST00000447027 P1958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:1257659 G>A maps to ENST00000447027 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr11:1256636 C>T maps to ENST00000447027 F961F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr11:1262891 G>A maps to ENST00000447027 R1597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr11:1264910 T>C maps to ENST00000447027 S2270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:1025322 C>T maps to NM_005961.2 G948G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:1017188 G>C maps to NM_005961.2 S1871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:1018513 G>T maps to NM_005961.2 A1429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr11:1021224 G>A maps to NM_005961.2 C1193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr11:1026119 C>T maps to NM_005961.2 W856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:20827488 T>A maps to NM_024544.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:105450668 G>A did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:105449468 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:105450779 A>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:105450802 G>C did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:105449900 A>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:105450999 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:105451325 A>G did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr9:103348697 G>T maps to NM_001018116.1 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:65630595 G>T maps to NM_025128.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:113547182 A>G maps to ENST00000189978 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:113563030 C>A maps to ENST00000189978 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:113563048 C>A maps to ENST00000189978 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:113549999 C>T maps to ENST00000189978 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:45797903 C>A maps to NM_001128425.1 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:88722557 C>G maps to NM_002461.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:110019346 C>T maps to NM_001114185.1 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr21:42807801 G>A maps to NM_001144925.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr21:42749717 G>T maps to NM_002463.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr23:3248703 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:3238787 C>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:3242717 G>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:3236018 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:3240742 C>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:3235315 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:3261853 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:3242836 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:3229351 T>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:3239839 T>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:3240620 T>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:3241208 T>A did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:3248134 A>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:3238836 G>T did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr23:3242790 T>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:3241308 T>G did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr23:3242455 G>T did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:3235499 C>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:3235238 T>C did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:3238594 T>C did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr17:74681209 C>T maps to NM_001008528.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr8:67488370 G>C maps to NM_001080416.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr20:42328596 G>T maps to NM_002466.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:42315649 C>T maps to NM_002466.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:102046454 G>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr12:102057288 T>A maps to NM_002465.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:102067296 C>A maps to NM_002465.2 I902I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr11:47355471 C>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:128750738 C>G maps to NM_002467.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:39330342 T>C maps to NM_012333.4 *104W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:77641897 G>A maps to NM_015057.4 I4091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr13:77835400 G>C maps to NM_015057.4 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr13:77657255 T>C maps to NM_015057.4 L3649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr13:77748549 T>A maps to NM_015057.4 T1849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr13:77743835 T>C maps to NM_015057.4 P1936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr13:77672486 T>C maps to NM_015057.4 E2934E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr13:77900607 C>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr13:77672951 C>T maps to NM_015057.4 L2779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr13:77740590 G>C maps to NM_015057.4 V2071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:77759383 G>A maps to NM_015057.4 Q1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr13:77636829 G>A maps to NM_015057.4 L4225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:16082518 C>T maps to NM_005378.4 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:16086029 C>T maps to NM_005378.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr2:16082410 G>T maps to NM_005378.4 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:153043009 G>A maps to NM_025107.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr6:153042994 G>A maps to NM_025107.2 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:69063186 G>A maps to NM_138768.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:241066129 G>T maps to NM_138336.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr12:81112733 C>A maps to NM_005593.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:81111129 G>T maps to NM_005593.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr12:81101698 C>A maps to NM_002469.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:81101809 G>A maps to NM_002469.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:10399722 G>A maps to NM_005963.3 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr17:10400463 G>T maps to NM_005963.3 R1526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:10411764 C>T maps to NM_005963.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:10399844 C>A maps to NM_005963.3 G1560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr16:15865567 A>G maps to NM_001040114.1 S304S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-18-4086-01A-01D-1352-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr16:15841518 G>C maps to NM_001040114.1 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr16:15831355 G>C maps to NM_001040114.1 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:15876248 G>T maps to NM_001040114.1 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr16:15853503 G>A maps to NM_001040114.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr16:15850287 C>G maps to NM_001040114.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:10235427 G>A maps to NM_003802.2 F762F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr17:10215276 C>T maps to NM_003802.2 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr17:10212955 C>A maps to NM_003802.2 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr17:10235417 T>A maps to NM_003802.2 K766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr17:10216512 C>T maps to NM_003802.2 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr17:10222448 G>C maps to NM_003802.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr17:10216042 C>A maps to NM_003802.2 E1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr17:10235463 G>T maps to NM_003802.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr19:50812386 G>T maps to NM_001145809.1 S1971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr19:50780013 G>T maps to NM_001145809.1 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:108147686 C>T maps to NM_014981.1 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr3:108183496 A>G maps to NM_014981.1 H593H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr3:108159978 C>T maps to NM_014981.1 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:10427836 G>A maps to NM_017534.5 I1707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:10429159 C>T maps to NM_017534.5 E1407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr17:10427842 T>C maps to NM_017534.5 R1705R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-22-4601-01A-01D-1441-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:10432231 C>A maps to NM_017534.5 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:10428930 G>T maps to NM_017534.5 I1458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr17:10431191 C>G did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr17:10543357 C>T maps to NM_002470.2 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:10542912 G>T maps to NM_002470.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:10549329 G>A maps to NM_002470.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr17:10543519 G>A maps to NM_002470.2 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr17:10356249 C>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr17:10364341 A>G maps to NM_017533.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:10355634 C>A maps to NM_017533.2 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr17:10348589 G>A maps to NM_017533.2 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr17:10360875 G>T maps to NM_017533.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:10353909 C>T maps to NM_017533.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr17:10352315 A>G maps to NM_017533.2 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr17:10352043 G>T maps to NM_017533.2 S1474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:10359022 C>A maps to NM_017533.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:23869530 C>T maps to NM_002471.3 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:23871778 C>T maps to NM_002471.3 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:23853812 C>T maps to NM_002471.3 E1801E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:23873973 G>T maps to NM_002471.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr14:23855702 G>T maps to NM_002471.3 R1594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:23858819 T>A maps to NM_002471.3 K1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:23873576 G>A maps to NM_002471.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:23866019 G>A maps to NM_002471.3 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr14:23894205 G>A maps to NM_000257.2 N817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr14:23884661 G>T maps to NM_000257.2 L1737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:23884401 T>C maps to NM_000257.2 E1787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr14:23887603 G>C maps to NM_000257.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:23894184 G>C maps to NM_000257.2 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr14:23886517 C>A maps to NM_000257.2 E1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr14:23889430 C>A maps to NM_000257.2 E1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr20:33582188 C>T maps to NM_020884.3 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:10296200 C>A maps to NM_002472.2 E1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:10304883 C>T maps to NM_002472.2 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr17:10307789 C>A maps to NM_002472.2 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:10312883 G>A maps to NM_002472.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr17:10315824 C>A maps to NM_002472.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:10298532 C>A maps to NM_002472.2 E1627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:10303704 A>G did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr22:36723504 C>T did not map to a codon.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr22:36681311 G>T maps to NM_002473.4 R1780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr7:101267538 C>A maps to NM_138403.4 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:44178573 G>A maps to ENST00000457314 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:44179955 G>C maps to ENST00000457314 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr20:35177600 C>T maps to NM_006097.3 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr6:16144052 C>T maps to NM_013262.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:123382997 C>T maps to NM_053025.3 E1313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:123452849 C>A maps to NM_053025.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr20:30419932 C>T maps to NM_033118.3 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr16:46771993 T>A maps to NM_182493.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:46741618 G>T maps to NM_182493.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr16:46781652 G>A maps to NM_182493.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:2679590 G>T maps to NM_001012418.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr6:2680467 C>A maps to NM_001012418.3 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr16:30387744 C>A maps to NM_013292.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:169501280 A>T maps to NM_018657.4 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:16769216 G>A maps to NM_012334.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:16818204 G>A maps to NM_012334.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:18039047 A>C maps to ENST00000205890 S1502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:18045065 C>A maps to ENST00000205890 Y1877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr17:18046881 G>A maps to ENST00000205890 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:18022929 A>G maps to ENST00000205890 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr13:109707449 A>G maps to NM_015011.1 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr13:109777484 G>A maps to NM_015011.1 Q1165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr13:109793151 C>A maps to NM_015011.1 S1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr13:109459127 C>G maps to NM_015011.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr13:109459145 T>C maps to NM_015011.1 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr17:27437116 G>A maps to NM_078471.3 D1030D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:26164575 G>A maps to ENST00000407587 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr22:26164470 T>C maps to ENST00000407587 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr22:26423088 G>T maps to ENST00000407587 R2385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr22:26164515 G>A maps to ENST00000407587 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr22:26351203 G>A maps to ENST00000407587 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:26219575 C>T maps to ENST00000407587 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr22:26164641 G>C maps to ENST00000407587 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr22:26422776 C>T maps to ENST00000407587 P2281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr17:34856769 C>G maps to NM_001163735.1 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:57440416 G>A maps to NM_005379.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr2:192206226 T>C maps to NM_001130158.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:192228558 C>A maps to NM_001130158.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:31098202 A>G maps to NM_015194.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr15:59516904 C>A maps to NM_004998.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:8609216 C>T maps to NM_012335.3 W496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:45004657 G>A maps to NM_033054.2 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:109835559 C>A maps to NM_001101421.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:109843824 C>T maps to NM_001101421.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr12:109835578 A>C maps to NM_001101421.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr10:26359048 C>T maps to NM_017433.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr10:26377271 G>T maps to NM_017433.4 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:171509591 T>C maps to NM_138995.3 F1329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:171073827 G>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:171238524 G>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:171225764 C>G maps to NM_138995.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:171509573 A>T maps to NM_138995.3 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:52700310 G>A maps to ENST00000358212 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr15:52718103 T>A maps to ENST00000358212 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:52720733 C>T maps to ENST00000358212 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:52622576 G>A maps to ENST00000358212 Q1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr15:52659306 C>A maps to ENST00000358212 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr18:47500811 G>T maps to NM_001080467.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:47404177 G>A maps to NM_001080467.2 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr18:47404252 C>A did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr18:47432925 C>T maps to NM_001080467.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:52497303 G>A maps to NM_018728.3 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr15:52564917 G>A maps to NM_018728.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr15:52561962 G>T maps to NM_018728.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr6:76550323 T>C maps to ENST00000428345 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:76580393 C>T maps to ENST00000428345 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr6:76580383 G>C maps to ENST00000428345 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr6:76582982 A>G maps to ENST00000428345 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:76867050 G>A maps to NM_000260.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:76869393 G>T maps to NM_000260.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr11:76893062 G>T maps to NM_000260.3 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr11:76922972 C>T maps to NM_000260.3 F2115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:76900493 C>G maps to NM_000260.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:76901869 C>G maps to NM_000260.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:128394439 G>A maps to ENST00000389524 A2068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:128324315 C>T maps to ENST00000389524 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:128394203 G>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:128389943 C>A maps to ENST00000389524 P1766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:128346006 C>A maps to ENST00000389524 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr15:72338532 C>T maps to ENST00000424560 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:17312970 G>C maps to NM_004145.3 L1565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:171621271 C>T maps to NM_000261.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:12655843 G>A maps to NM_001146312.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:12642620 C>A maps to NM_001146312.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr17:12666801 C>A maps to NM_001146312.1 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:12664014 G>T maps to NM_001146312.1 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr11:17742501 C>T maps to NM_002478.4 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:17741694 G>A maps to NM_002478.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:17741679 C>A maps to NM_002478.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr11:17741490 C>A maps to NM_002478.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:203054777 C>T maps to NM_002479.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:203054888 C>T maps to NM_002479.4 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr18:3116505 C>T maps to NM_003803.3 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:3086146 C>A maps to NM_003803.3 V1380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:3086125 A>G maps to NM_003803.3 T1387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr8:2026940 G>T maps to NM_003970.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:2024290 C>T maps to NM_003970.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:2057232 C>A maps to NM_003970.2 R1031R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:24418728 G>T maps to ENST00000330966 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:24384006 C>G maps to ENST00000330966 G1390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:24400708 G>C maps to ENST00000330966 S971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr10:75393824 T>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:120107145 G>T maps to NM_016599.3 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr5:150042511 C>A maps to NM_133371.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr10:69935097 G>A maps to NM_032578.2 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr10:69935178 G>A maps to NM_032578.2 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr10:69881320 C>T maps to NM_032578.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr10:69961673 C>T maps to NM_032578.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr3:40286055 G>A maps to NM_015460.2 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:40231920 C>T maps to NM_015460.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:40231545 G>A maps to NM_015460.2 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:31131697 C>T maps to NM_182958.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr16:31141587 G>T maps to NM_182958.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr16:31141396 C>T maps to NM_182958.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:47886479 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:41800487 G>A maps to NM_006766.3 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:41834526 T>A maps to NM_006766.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr8:41798402 G>C maps to NM_006766.3 S999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr8:41804151 A>C maps to NM_006766.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:41798769 C>A maps to NM_006766.3 E877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:41834548 G>C maps to NM_006766.3 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:41792161 G>A maps to NM_006766.3 I1192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr10:76790710 C>T maps to NM_012330.2 H2043H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:62842682 C>T maps to NM_004535.2 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:62871198 G>A maps to NM_004535.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:1906879 C>T maps to ENST00000399161 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:1921046 G>A maps to ENST00000399161 H516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:1805476 G>A maps to ENST00000399161 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:1796158 G>A maps to ENST00000399161 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:1843123 G>T maps to ENST00000399161 C959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:1893047 G>T maps to ENST00000399161 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:1926493 C>T maps to ENST00000399161 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:1927026 G>A maps to ENST00000399161 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr16:48596133 G>A maps to NM_153029.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:40123492 A>G maps to NM_018177.3 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:40099025 T>G maps to NM_018177.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr13:33002141 G>A maps to NM_052818.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr13:33110056 C>A maps to ENST00000505213 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr13:21331601 C>A maps to NM_174928.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:153195636 C>T did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:153195480 C>G did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:80246827 C>A maps to NM_032693.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr4:140264006 C>T maps to NM_057175.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:140291422 G>A maps to NM_057175.3 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:112499078 C>T maps to NM_024953.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr12:112481016 T>A did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr12:112478341 T>C maps to NM_024953.3 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr12:112486192 C>A maps to NM_024953.3 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr12:112481659 T>C maps to NM_024953.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:57857945 G>T maps to NM_001011713.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr4:76852391 C>T maps to NM_014435.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:89911208 G>A maps to NM_005467.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:89892409 C>A maps to NM_005467.3 Y298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:89891311 G>A did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:89911208 G>A maps to NM_005467.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:89907063 G>T maps to NM_005467.3 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:64813811 C>A maps to ENST00000340252 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:174815048 A>C maps to NM_207015.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr3:175165047 C>T maps to NM_207015.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:175520972 C>G maps to NM_207015.2 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:191524441 C>T maps to NM_005966.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr17:59668328 C>G maps to NM_199290.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:71189498 C>A maps to NM_018161.4 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:164087747 T>C maps to NM_138386.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:164050299 G>A maps to NM_138386.2 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:164054360 C>T maps to NM_138386.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:71305463 G>A maps to NM_017567.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr2:71305574 G>A maps to NM_017567.4 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr13:101881752 C>A maps to NM_052867.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr13:101714325 G>T maps to NM_052867.2 I1583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr13:101763504 G>A maps to NM_052867.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr13:101763489 G>A maps to NM_052867.2 I760I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr13:101997646 C>A maps to NM_052867.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr13:101753187 G>A maps to NM_052867.2 Q1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr13:101756666 T>A maps to NM_052867.2 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:7942324 C>T maps to NM_024865.2 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:46417621 C>A maps to NM_001029861.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr19:13988532 G>A maps to NM_001098622.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:25596914 C>A maps to NM_152667.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:72433580 T>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:72433466 C>G did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:72434096 C>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:72433073 C>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:72433379 G>C did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:72433952 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:72433990 A>T did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:92927344 T>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:92928263 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:92927475 T>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:92927280 C>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:92927455 C>A did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr23:92927258 T>G did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:92927281 G>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:2985953 G>A maps to ENST00000399624 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:47991583 G>A maps to NM_003827.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:23361891 T>C maps to ENST00000431864 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr18:10532792 G>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:50865268 G>C maps to NM_004851.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr16:780536 C>T maps to NM_022493.1 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr16:789702 C>T maps to NM_022493.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:34158540 G>T maps to NM_024662.2 G727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:18258272 G>T maps to NM_000015.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:73927787 G>A maps to NM_016347.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:201751847 G>T maps to ENST00000367296 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:201757713 G>A maps to ENST00000367296 E1038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:20070276 C>T maps to ENST00000396087 L1325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:19970368 C>T maps to ENST00000396087 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr11:20057594 C>T maps to ENST00000396087 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:20057510 C>T maps to ENST00000396087 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:78511808 G>A maps to NM_014903.4 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:78444759 G>C maps to NM_014903.4 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr12:78510560 C>T maps to NM_014903.4 D882D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr12:78400572 G>T maps to NM_014903.4 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr12:78400649 T>A maps to NM_014903.4 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr12:78513707 C>T maps to NM_014903.4 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:78400814 C>G maps to NM_014903.4 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:78582543 T>A maps to NM_014903.4 T1992T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:78542699 G>T did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:78400497 C>A maps to NM_014903.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:78513395 C>G maps to NM_014903.4 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:78515842 G>T maps to NM_014903.4 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr12:78400702 T>A maps to NM_014903.4 L462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr12:78593180 A>G maps to NM_014903.4 K2173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:78582516 C>A maps to NM_014903.4 Y1983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr12:78534060 G>T did not map to a codon.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr12:78400259 T>A maps to NM_014903.4 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:78515827 C>A maps to NM_014903.4 G1286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:78562612 G>T maps to NM_014903.4 G1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:15415805 G>A maps to NM_015909.2 S1842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:15679376 G>T maps to NM_015909.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:15564443 G>T maps to NM_015909.2 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:15449303 G>T maps to NM_015909.2 A1550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr2:15607789 G>A maps to NM_015909.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:15519751 G>C maps to NM_015909.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:15676579 G>A maps to NM_015909.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:15417011 G>A maps to NM_015909.2 H1784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:15374742 C>A maps to NM_015909.2 V2024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr13:36124677 C>G maps to ENST00000400445 S2217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr13:35923290 G>T maps to ENST00000400445 E1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr13:35769998 A>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr13:35733367 C>T maps to ENST00000400445 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr13:36026232 G>T maps to ENST00000400445 T2103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr13:35517157 C>T maps to ENST00000400445 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr13:35864574 G>T maps to ENST00000400445 L1942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:47044476 C>A maps to NM_015175.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:47030751 G>T maps to NM_015175.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr8:90965858 A>G maps to NM_002485.4 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:16902815 G>A maps to NM_017940.3 Q689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:16902855 C>A maps to NM_017940.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:16902792 C>A maps to NM_017940.3 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:16907279 G>T maps to NM_017940.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:16893673 C>A maps to NM_017940.3 E947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:148004763 T>C maps to ENST00000310701 E855E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr1:21804672 G>A maps to NM_032264.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:120384084 G>C maps to NM_001047980.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:120384191 G>T maps to NM_001047980.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:113102369 C>T maps to ENST00000316851 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr21:22746205 C>A maps to NM_004540.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:22849674 G>T maps to NM_004540.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr21:22881367 T>A maps to NM_004540.2 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr21:22746193 C>T maps to NM_004540.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr21:22804458 C>A maps to NM_004540.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr21:22910193 G>A maps to NM_004540.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr19:19344640 G>C maps to NM_004386.2 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:19337670 C>T maps to NM_004386.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr19:19345810 C>A maps to NM_004386.2 C1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr19:19338798 G>A maps to NM_004386.2 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr12:6637953 C>T maps to NM_014865.3 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr11:134038016 G>A maps to NM_015261.2 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr4:17824746 G>C did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:158439182 C>A maps to NM_017760.5 G1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr7:158438253 C>A maps to NM_017760.5 V1079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:158464253 T>G maps to NM_017760.5 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:74197369 G>A maps to NM_000265.4 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:183525255 G>C maps to NM_001127651.2 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:183559389 G>T maps to NM_001127651.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr22:37260121 C>A maps to NM_013416.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:136664722 G>T maps to NM_006153.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr3:136646960 C>T maps to NM_006153.4 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:183902799 G>A maps to NM_205842.1 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:183866997 C>T did not map to a codon.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr12:54903645 C>T maps to NM_005337.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr12:54905760 C>T maps to NM_005337.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr12:54903515 G>T maps to NM_005337.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:133541728 G>A maps to NM_207363.2 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:133539727 T>C maps to NM_207363.2 K1552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:133540267 G>A maps to NM_207363.2 I1372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:133539997 C>A maps to NM_207363.2 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:133489453 G>A maps to NM_207363.2 Q1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr2:133636485 C>A maps to NM_207363.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:50187174 C>T maps to NM_001037806.3 E1100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:50185657 G>C maps to NM_001037806.3 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr12:50196739 C>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:24930636 G>C maps to NM_003743.4 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr2:24949569 A>T maps to NM_003743.4 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:24985566 C>G maps to NM_003743.4 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:24930642 G>T maps to NM_003743.4 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:24929796 C>T maps to NM_003743.4 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr8:71078965 C>A maps to NM_006540.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr8:71044151 G>A maps to NM_006540.2 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:71071770 G>A maps to NM_006540.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr8:71075034 C>T maps to NM_006540.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr8:71075760 G>T maps to NM_006540.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr10:51582220 A>T maps to NM_001145260.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr20:33329844 C>A maps to NM_014071.2 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr20:33345833 T>A maps to NM_014071.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr20:33328761 C>T maps to NM_014071.2 L1766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr17:16068451 A>G maps to ENST00000395857 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr17:15952253 G>T maps to ENST00000395857 Y2162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:16068380 G>C maps to ENST00000395857 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr17:15978953 C>A maps to ENST00000395857 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:16029510 G>T maps to ENST00000395857 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:124915225 G>T maps to NM_006312.4 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr12:124840061 T>A maps to NM_006312.4 P1106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:124950784 G>C maps to NM_006312.4 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:124979764 C>A maps to NM_006312.4 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:124848271 G>A maps to NM_006312.4 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr19:55418049 A>G maps to NM_004829.5 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr19:55421425 G>T did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr6:31556855 G>A maps to NM_147130.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:160322954 C>T maps to NM_015331.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:160314556 T>A maps to NM_015331.2 L44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:160319458 T>C maps to NM_015331.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr18:2585113 A>T maps to NM_006101.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr18:2577813 G>T maps to NM_006101.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:8351895 G>T maps to ENST00000402554 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr15:23931854 C>G maps to NM_002487.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr15:23931539 G>T maps to NM_002487.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr15:23931527 C>A maps to NM_002487.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr15:23932118 G>T maps to NM_002487.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:43809126 C>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr10:75567216 G>A maps to NM_003635.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr4:118975202 G>A maps to NM_004784.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr4:115773881 T>C maps to NM_022569.1 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr4:115858644 T>C maps to NM_022569.1 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr4:115858508 G>T maps to NM_022569.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:115891699 C>A maps to NM_022569.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr4:115997761 G>T maps to NM_022569.1 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:240929489 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:240900567 G>A maps to ENST00000404554 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr12:4763617 C>T maps to NM_005002.4 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr12:4791397 G>T maps to NM_005002.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr6:97339015 G>A maps to NM_014165.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr3:179334807 C>T maps to NM_002492.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:14682709 T>A maps to NM_004146.4 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:161179711 A>T maps to NM_004550.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:67800725 C>T maps to NM_002496.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:67800459 G>T maps to NM_002496.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:67379865 G>A maps to NM_007103.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:152348669 C>T maps to NM_001164507.1 Q8333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:152512795 G>C maps to NM_001164507.1 V2122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:152512351 C>T maps to NM_001164507.1 Q2227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:152525606 C>T maps to NM_001164507.1 K1515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:152403999 A>C maps to NM_001164507.1 S6770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:152553724 G>A maps to NM_001164507.1 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:152521923 C>A maps to NM_001164507.1 E1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:152410491 G>A maps to NM_001164507.1 I6492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr2:152410491 G>A maps to NM_001164507.1 I6492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr2:152382498 G>C maps to NM_001164507.1 V7378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:152373008 G>A maps to NM_001164507.1 Y7623Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:152580772 C>A did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr10:21169794 G>A maps to ENST00000430741 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr10:21097436 A>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:84024220 G>A maps to NM_019065.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr16:84014677 C>T maps to NM_019065.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:8242615 C>A maps to NM_015509.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr1:16775692 C>T maps to NM_018090.4 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr12:97328809 G>T maps to NM_001135175.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr15:56152936 C>A maps to ENST00000508342 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr15:56144620 C>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr18:56033436 C>T maps to NM_001144967.1 Y680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr18:56009013 A>G maps to NM_001144967.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr6:11185598 C>T maps to NM_006403.3 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:11185538 G>C maps to NM_006403.3 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr22:29884888 C>T maps to NM_021076.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:24811164 G>A maps to ENST00000221169 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:72076746 C>T maps to NM_173808.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:72748156 C>A maps to NM_173808.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr8:11640744 G>T maps to NM_145043.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:11637322 G>T maps to NM_145043.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:178260983 A>T maps to NM_018248.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr4:178272638 G>T maps to NM_018248.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr4:178272629 C>T maps to NM_018248.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:130852746 T>C maps to NM_024800.4 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:211836893 G>C maps to NM_002497.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr17:27062331 G>A maps to NM_178170.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr17:27066121 G>A maps to NM_178170.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:75574084 G>A maps to NM_033116.4 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr14:75590748 C>A maps to NM_033116.4 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:20699476 G>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:21556040 G>C maps to NM_006157.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:20940810 C>A maps to NM_006157.3 C230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:21596534 T>C maps to NM_006157.3 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:20940795 A>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:45097608 G>A maps to NM_001145107.1 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:44913928 C>A maps to NM_001145107.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:73418809 C>G maps to NM_002499.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:156642659 G>A maps to NM_006617.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:156641285 C>T maps to NM_006617.1 W898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:156639956 G>T maps to NM_006617.1 G1341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:156640163 G>T maps to NM_006617.1 P1272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:5498920 C>T maps to NM_001047160.1 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:5495513 C>A maps to NM_001047160.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:70532041 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:70532459 G>T maps to NM_153181.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr18:70417576 G>T maps to NM_153181.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr18:70417778 C>T maps to NM_153181.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr18:70532106 G>T maps to NM_153181.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:31828011 G>A maps to NM_000434.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr2:233899700 C>T maps to NM_005383.2 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:233899556 C>G maps to NM_005383.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:242757899 C>A maps to NM_001167599.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr10:105344806 C>T maps to NM_004210.4 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr20:44517425 C>A maps to NM_080749.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr17:7232367 G>A maps to NM_032442.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:7221431 C>A maps to NM_032442.2 E1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:182542873 A>G maps to NM_002500.2 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:182543311 A>T maps to NM_002500.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:37762557 C>A maps to NM_006160.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:31377976 C>T maps to NM_022728.2 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr7:31378048 G>T maps to NM_022728.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:31378806 C>A maps to NM_022728.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:113436085 C>A maps to NM_024019.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:29483113 C>T maps to NM_001042492.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr17:29527582 A>G maps to NM_001042492.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:29556344 T>A maps to NM_001042492.2 C904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:29670024 A>G did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr17:29664884 G>T maps to NM_001042492.2 E2231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:29685527 C>A maps to NM_001042492.2 T2667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr17:29679290 C>T maps to NM_001042492.2 Q2492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:29527557 G>A maps to NM_001042492.2 W336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr17:29663349 G>T did not map to a codon.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr17:29665756 C>A maps to NM_001042492.2 Y2285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr22:30035116 C>A maps to NM_181832.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:30070891 C>T maps to NM_181832.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr22:30035097 C>G maps to NM_181832.2 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:204951101 G>A maps to ENST00000367172 G808G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:204951141 G>T maps to ENST00000367172 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr16:69727790 C>T maps to NM_138713.2 Q1355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:77211799 C>T maps to NM_172387.1 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:77170979 G>T maps to NM_172387.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr18:77193659 C>G maps to NM_172387.1 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr18:77246386 C>T maps to NM_172387.1 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr20:50049291 G>A maps to NM_012340.3 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:50071199 G>A maps to NM_012340.3 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr16:28970372 G>T maps to NM_032815.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr16:28967598 C>T maps to NM_032815.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:24842949 C>A maps to NM_001136022.1 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:54686871 A>T maps to NM_001136023.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:46135877 C>T maps to ENST00000362042 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr17:46135697 T>C maps to ENST00000362042 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:61554057 G>T maps to NM_001145512.1 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:14307057 G>T maps to ENST00000397581 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr9:14307520 T>C did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr9:14307381 T>A maps to ENST00000397581 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:13136139 G>A maps to ENST00000397661 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr4:103498031 G>T did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr8:145659004 C>T maps to NM_013432.4 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr8:145664052 G>T maps to NM_013432.4 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr8:145667758 G>C maps to NM_013432.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr8:145663859 C>T maps to NM_013432.4 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:101574240 G>A maps to NM_031419.3 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:129762614 C>A maps to NM_006165.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr9:33318766 G>T maps to NM_002504.4 G543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr4:47857074 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:104515089 C>A maps to NM_006166.3 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:233785169 C>A maps to NM_019850.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr17:47583904 C>T maps to NM_002507.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:90814722 G>T maps to NM_001033088.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr4:103822327 G>C maps to NM_139173.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:103966045 C>A did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr13:39621262 C>T maps to NM_001012754.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr22:42071110 C>T maps to ENST00000402458 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr23:17746084 G>T did not map to a codon.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr23:17746388 C>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:17746068 C>T did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:17739651 A>G did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:17750481 C>G did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:17394301 A>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:17744704 C>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:17750514 C>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:17745611 C>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:17745562 C>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:17743831 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:17750109 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:71359732 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:71360442 C>G did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:236189397 G>A maps to NM_002508.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:236208959 T>C maps to NM_002508.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:52534584 G>T maps to NM_007361.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr14:52534713 C>T maps to NM_007361.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:52478331 G>T maps to NM_007361.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr14:52520918 C>A maps to NM_007361.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr14:52534596 G>A maps to NM_007361.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:51219372 C>A maps to NM_020921.3 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr14:51190285 T>A maps to NM_020921.3 A2099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:675284 C>T maps to NM_016533.4 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr20:25493535 C>T maps to NM_025176.4 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr15:23049065 C>T maps to NM_144599.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr8:99248400 T>A maps to NM_024759.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:24766702 C>T maps to NM_020448.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:24795599 C>A maps to NM_020448.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr5:37000925 G>A maps to NM_133433.3 R1170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:37000523 A>G maps to NM_133433.3 E1118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr5:36985486 T>C maps to NM_133433.3 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr9:107535352 A>T maps to NM_018376.2 *248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:52525431 C>A maps to NM_007184.3 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr3:52526101 C>G maps to NM_007184.3 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:100065091 A>C maps to NM_020202.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:100064426 A>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:124676410 A>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:125139576 C>T maps to NM_001040214.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:119064020 A>C did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:119077306 G>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:119070582 G>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:28227292 T>C maps to NM_001007531.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr6:28228141 C>A maps to NM_001007531.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:51875031 C>T maps to NM_005601.3 *166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:40174624 G>A maps to ENST00000316082 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr19:45656362 C>T maps to NM_198478.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:118724760 C>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:118724822 C>A did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:118723941 C>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:118724196 A>G did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:42679872 C>T maps to NM_005385.3 R893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:36986503 C>T maps to NM_001079668.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:21494121 C>T maps to NM_002509.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:134598852 G>T maps to NM_177400.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr8:41504000 G>A maps to ENST00000425142 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:33463217 C>T maps to NM_018096.3 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:173525587 C>T maps to NM_014932.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:173525584 G>T maps to NM_014932.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:173999026 A>G maps to NM_014932.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:173998630 G>A maps to NM_014932.2 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:173993317 G>T did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr3:173996792 A>G maps to NM_014932.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:173997008 A>T maps to NM_014932.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:70389466 G>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:70389332 A>G did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:70386934 T>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:70389918 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:70389550 C>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:70389798 C>A did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:5811255 G>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:5811207 C>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:5821720 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:5811525 G>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:5810953 T>G did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:5827146 C>A did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr23:5821714 G>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:5811061 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:5821360 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:6069166 A>T did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:5821840 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:5821117 C>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:5821665 G>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr24:16952690 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr24:16953004 C>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr24:16952513 C>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr17:26518100 C>T maps to NM_016231.4 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:3613665 A>T maps to ENST00000448023 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr16:3593453 C>T maps to ENST00000448023 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:32475783 T>C maps to NM_021209.4 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:32449810 G>A maps to NM_021209.4 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:32449822 C>A maps to NM_021209.4 G932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:32477620 G>T maps to NM_021209.4 C43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr17:5433897 T>C maps to NM_033004.3 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:7981633 C>A maps to NM_176821.3 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr11:7982312 T>A maps to NM_176821.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr11:7982579 A>G maps to NM_176821.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:7981751 G>A maps to NM_176821.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56329492 C>T maps to NM_145007.3 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr19:56320535 C>T maps to NM_145007.3 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr19:56320724 G>C maps to NM_145007.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:56321462 G>A maps to NM_145007.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:54301540 C>G maps to ENST00000391773 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:54313685 C>A maps to ENST00000391773 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:54313982 C>T maps to ENST00000391773 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:54313592 C>A maps to ENST00000391773 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56423075 G>A maps to NM_176810.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56423565 G>A maps to NM_176810.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56423895 C>T maps to NM_176810.2 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:56423243 C>A maps to NM_176810.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:56436387 G>C maps to NM_176810.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:56419213 A>T maps to NM_176810.2 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:56424443 G>A maps to NM_176810.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:56423148 T>C maps to NM_176810.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:7081199 G>T maps to NM_176822.3 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:7064864 G>A maps to NM_176822.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr11:7079555 T>C maps to NM_176822.3 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:55493719 G>A maps to NM_017852.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:55494235 C>A maps to NM_017852.3 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:55493894 C>T maps to NM_017852.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:247607427 A>T maps to NM_004895.4 K942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:247588562 G>A maps to NM_004895.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:247607403 G>T maps to NM_004895.4 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:247588865 C>A maps to NM_004895.4 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:247588745 C>A maps to NM_004895.4 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:247582272 C>A maps to NM_004895.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr1:247588142 C>A maps to NM_004895.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56363640 A>G maps to NM_134444.4 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56369415 C>T maps to NM_134444.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:56369236 G>T maps to NM_134444.4 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:56372848 G>T maps to NM_134444.4 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr19:56369052 C>A maps to NM_134444.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr19:56363670 C>A maps to NM_134444.4 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:56369841 G>T maps to NM_134444.4 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56515201 C>T maps to NM_153447.4 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56569656 C>T maps to NM_153447.4 A1117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:56549481 G>T maps to NM_153447.4 G903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr19:56539872 A>G maps to NM_153447.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:56539487 C>A maps to NM_153447.4 S630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:56539854 A>G maps to NM_153447.4 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:281740 A>C maps to NM_138329.1 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr19:55447726 C>T maps to ENST00000446217 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:55451775 G>T maps to ENST00000446217 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:55450740 C>T maps to ENST00000446217 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr19:55451046 C>T maps to ENST00000446217 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:55452950 C>T maps to ENST00000446217 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:55450739 C>A maps to ENST00000446217 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:55451508 C>T maps to ENST00000446217 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:56487654 A>G maps to NM_176811.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:56487501 G>A maps to NM_176811.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:56467200 C>T maps to NM_176811.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr19:56481993 A>C maps to NM_176811.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:56487669 G>C did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:56485170 T>A maps to NM_176811.2 C896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:56243489 G>A maps to NM_176820.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:142400041 T>C did not map to a codon.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr3:160952597 A>G maps to ENST00000472947 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr3:160952513 G>T did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr17:49239124 A>G maps to NM_198175.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:152132273 G>A maps to NM_004688.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr2:152139422 C>A maps to NM_004688.2 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:139297772 G>T maps to ENST00000296202 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr4:56471491 G>A maps to NM_006681.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr4:56496628 T>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:56465342 C>T maps to NM_006681.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr5:151784572 G>A maps to NM_020167.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:43675645 G>T maps to NM_182977.2 G890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr5:43649384 G>C maps to NM_182977.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr7:144097349 A>G maps to ENST00000467773 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:880524 C>A maps to NM_015658.3 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr10:96121572 G>A maps to NM_022451.9 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:132635871 C>T maps to NM_024078.1 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr7:30492390 C>T maps to NM_006092.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:30492414 C>T maps to NM_006092.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:30492315 G>A maps to NM_006092.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:30491409 G>A maps to NM_006092.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:30492087 G>A maps to NM_006092.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:50744673 C>T maps to NM_022162.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr16:50745777 G>A maps to NM_022162.1 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr16:50744940 T>A maps to NM_022162.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:50759417 C>G maps to NM_022162.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr16:50745744 C>A maps to NM_022162.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr18:31432873 G>T maps to NM_003787.4 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr18:31673471 T>C maps to NM_003787.4 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr18:31463289 G>T maps to NM_003787.4 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:6592773 G>T maps to NM_024654.4 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:103920359 G>C maps to ENST00000405356 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:103921373 G>A maps to ENST00000405356 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:103921911 G>A maps to ENST00000405356 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:103920563 A>G maps to ENST00000405356 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:156742847 G>T maps to NM_138400.1 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr7:156743220 G>T maps to NM_138400.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr16:14960469 G>T maps to ENST00000456867 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:70511813 A>C did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr4:2944034 C>T maps to NM_003703.1 S645S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-21-5786-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr5:175815444 C>T maps to ENST00000503175 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr12:117672550 G>A maps to ENST00000338101 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr12:117718547 G>T maps to ENST00000338101 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr12:117669886 G>A maps to ENST00000338101 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:117672399 C>A maps to ENST00000338101 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:117658043 G>A maps to ENST00000338101 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:162335297 C>T maps to NM_014697.2 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:26107881 G>A maps to NM_000625.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr17:26110056 C>A maps to NM_000625.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr7:150696173 G>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr7:150698696 A>G maps to NM_000603.4 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:150698428 C>A maps to NM_000603.4 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr9:139405213 C>A maps to NM_017617.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr9:139412362 T>A maps to NM_017617.3 K428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr9:139390778 G>T maps to NM_017617.3 S2471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:139391109 G>A maps to NM_017617.3 Q2361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:139397646 G>A maps to NM_017617.3 I1718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:139391558 G>C maps to NM_017617.3 S2211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr9:139397637 C>A maps to NM_017617.3 V1721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:139402783 C>T maps to NM_017617.3 W1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:120468264 G>A maps to NM_024408.2 Q1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:120512257 G>A maps to NM_024408.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr1:120506350 A>G maps to NM_024408.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr1:145282030 G>C maps to ENST00000454606 *249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:145281549 C>T maps to ENST00000454606 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:145281549 C>T maps to ENST00000454606 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:145273191 G>T maps to ENST00000454606 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:15281269 G>C maps to NM_000435.2 V1662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr19:15273332 C>T maps to NM_000435.2 V1952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:32163486 G>A maps to NM_004557.3 G1913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:32185862 C>T maps to NM_004557.3 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:79914613 C>T maps to NM_178493.5 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr17:79911085 C>T maps to NM_178493.5 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:120431545 G>A maps to NM_002514.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr8:120431548 G>T maps to NM_002514.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr14:26949314 C>A maps to ENST00000449198 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr14:26917693 A>T maps to ENST00000449198 L349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:46443309 C>T maps to NM_002516.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:100118221 C>T did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr23:100117752 C>T did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:100117171 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:155761199 C>T maps to NM_015718.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr6:155761238 T>G maps to NM_015718.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:89073305 T>C maps to NM_016931.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:89069062 T>A maps to NM_016931.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr11:89075239 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:69339853 C>T maps to NM_024505.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr15:69323868 C>T maps to NM_024505.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:101582166 C>T maps to NM_002518.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:101604629 A>T maps to NM_002518.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:33684438 G>A maps to NM_001164749.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr11:66191620 T>C maps to NM_178864.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr11:66191303 A>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:66191326 C>T maps to NM_178864.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:108047021 T>A maps to NM_002519.2 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:108057294 C>A maps to NM_002519.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr20:62737383 G>A maps to NM_005286.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:62737587 C>G maps to NM_005286.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr20:62737572 G>C maps to NM_005286.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr18:21123434 A>T maps to NM_000271.4 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr7:44560415 G>T maps to NM_013389.2 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:44555411 G>A maps to NM_013389.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr7:44571704 G>A maps to NM_013389.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr7:44556481 G>C maps to NM_013389.2 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:44556513 C>A maps to NM_013389.2 E1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:72026001 C>A maps to ENST00000277942 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:110926115 G>T maps to NM_000272.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:110886761 C>T did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:132440893 G>A maps to ENST00000393156 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr3:132432079 G>A maps to ENST00000393156 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr3:132419236 C>A maps to ENST00000393156 G562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr3:132400855 G>C maps to ENST00000393156 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:5993283 G>A maps to NM_015102.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:5964864 C>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:36333108 G>A maps to NM_004646.3 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:36335227 G>C maps to NM_004646.3 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr19:36333141 C>G maps to NM_004646.3 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:36342188 A>G maps to NM_004646.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr19:36335016 G>A maps to NM_004646.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:36339014 C>A maps to NM_004646.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:179520316 G>T maps to NM_014625.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:21882971 G>T maps to NM_182795.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr4:106888365 C>A maps to ENST00000503451 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:11918370 G>T maps to NM_002521.2 Y96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:153659830 C>A maps to NM_000906.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:153658630 T>C maps to NM_000906.3 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:153658606 C>T maps to NM_000906.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:153652174 C>T maps to NM_000906.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:35807325 G>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr9:35793035 G>T maps to NM_003995.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:34851431 C>T maps to NM_207172.1 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:34851422 C>T maps to NM_207172.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:98254456 C>T maps to NM_002523.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr22:39224454 G>A maps to NM_014293.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:24329196 C>A maps to NM_000905.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:164247529 C>A maps to NM_000909.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:164247166 A>C maps to NM_000909.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr4:164247496 C>T maps to NM_000909.4 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:164271901 G>C maps to NM_006174.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr4:164271505 C>T maps to NM_006174.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:69748869 G>A maps to NM_000903.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:30326501 C>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:30327184 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:30326749 C>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:30327352 C>A did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:30326571 G>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:50885781 G>T maps to NM_007121.4 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:47290246 A>T maps to NM_005693.2 *448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:100928737 C>G maps to ENST00000392986 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr6:108492768 C>T maps to ENST00000368983 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:108501624 T>A did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr6:108497812 G>A maps to ENST00000368983 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr5:142680224 C>A maps to NM_001024094.1 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:149357658 G>T maps to ENST00000511528 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr4:149075780 G>A maps to ENST00000511528 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:52451219 G>A maps to ENST00000360284 W536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr2:157186680 C>T maps to NM_006186.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr9:102626001 C>A maps to NM_173200.1 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr9:102590725 C>A maps to NM_173200.1 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:102607052 T>A maps to NM_173200.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:127245162 C>T maps to NM_004959.4 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:200017934 A>T maps to NM_205860.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr10:115350344 G>A maps to ENST00000369358 Q1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:115374674 G>A maps to ENST00000369358 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr10:115412756 G>A maps to ENST00000369358 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr10:115365537 C>A maps to ENST00000369358 G1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:115392841 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr10:115423109 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:115348835 C>G maps to ENST00000369358 R1705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr9:140196232 C>A maps to NM_001004354.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr9:140196056 C>T maps to NM_001004354.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:115256590 G>T maps to NM_002524.3 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:64893253 C>A maps to NM_030759.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:27659660 G>T maps to ENST00000379863 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr7:107824714 T>C maps to ENST00000379032 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr7:107822331 G>T maps to ENST00000379032 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:107824690 C>T maps to ENST00000379032 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr8:32463184 C>A maps to NM_013956.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:32621847 C>A maps to NM_013956.3 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr8:32616828 C>T maps to NM_013956.3 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:32617715 A>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:32621880 G>T maps to NM_013956.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr10:84745016 G>T maps to ENST00000404547 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr10:84745279 G>T maps to ENST00000404547 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr10:84118600 G>A maps to ENST00000404547 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:16337375 G>A maps to NM_003489.3 I1046I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr21:16337171 C>T maps to NM_003489.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr21:16338047 C>T maps to NM_003489.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr12:2943894 G>C maps to NM_031474.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr12:2943846 C>T maps to NM_031474.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:105152884 C>A did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:105167218 C>T did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:105075046 G>A did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:105149284 C>G did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:105152798 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:105153310 G>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:105153422 A>G did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:105153116 C>G did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:105178434 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:105153577 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:105189946 A>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:105187984 C>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:105179164 A>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:105152719 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:105190365 A>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:105153032 C>G did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:105168795 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:105139490 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:105169002 G>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:105152980 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:105166012 C>G did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:105075070 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:105183975 G>T did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr6:6002584 C>G did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr10:33559684 C>A maps to NM_003873.5 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:33552638 G>C maps to NM_003873.5 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr10:33543122 C>A did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:206631515 C>A maps to NM_201266.1 S805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr2:206562428 G>T maps to NM_201266.1 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr6:24146059 C>T maps to NM_080723.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:50280564 C>G maps to ENST00000404971 V1364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr2:50723175 T>C maps to ENST00000404971 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:50847249 A>T maps to ENST00000404971 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:50573835 G>T maps to NM_138735.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:51253553 G>A maps to ENST00000404971 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:50723112 G>T maps to ENST00000404971 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:50149180 T>C maps to ENST00000404971 S1515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr2:50149152 C>A maps to ENST00000404971 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:50724616 G>A maps to ENST00000404971 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:50733743 C>A maps to ENST00000404971 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:50765610 C>A maps to ENST00000404971 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64434782 G>A maps to NM_015080.3 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64436052 G>A maps to NM_015080.3 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr11:64427951 G>A maps to NM_015080.3 N747N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:64453120 G>T maps to NM_015080.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr11:64402789 G>T maps to NM_015080.3 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr11:64374838 G>A maps to NM_015080.3 A1656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:64418068 A>T maps to NM_015080.3 L987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:64434731 A>G maps to NM_015080.3 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:80164195 A>G maps to NM_004796.4 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:79434663 C>T maps to NM_004796.4 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr14:79432743 C>A maps to NM_004796.4 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr5:176637415 A>T maps to NM_022455.4 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:176638019 G>T maps to NM_022455.4 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr5:176696630 C>T maps to NM_022455.4 R1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr5:176678729 G>C did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr5:176673710 C>T maps to NM_022455.4 R1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr23:152037558 G>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr17:44770426 A>C maps to NM_006178.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr17:44806224 C>T maps to NM_006178.2 Y611Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:59510036 T>C maps to NM_001144772.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr8:59506794 G>A maps to NM_001144772.1 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:59510090 C>T maps to NM_001144772.1 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr16:27238085 G>A maps to NM_145080.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:27246602 T>A maps to NM_145080.3 K52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr5:6602599 G>A maps to NM_017755.5 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:6600125 T>A maps to NM_017755.5 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr5:6620366 G>A maps to NM_017755.5 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:6620316 G>C maps to NM_017755.5 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:40124969 A>T maps to NM_032526.1 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:40126837 C>A maps to NM_032526.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:18745241 G>T maps to ENST00000455492 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr2:18768394 G>C maps to ENST00000455492 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:18765907 G>A maps to ENST00000455492 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr7:33061711 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:116544292 C>A maps to NM_152729.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:52563207 C>T maps to NM_001134231.1 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr3:52562309 C>T maps to NM_001134231.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:104190719 G>C maps to NM_001031701.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr6:86201752 T>C maps to NM_002526.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr6:86181078 C>A maps to NM_002526.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr6:86181075 C>A maps to NM_002526.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:86201764 C>A maps to NM_002526.2 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:5603967 G>A maps to NM_001102654.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:49564642 G>C maps to NM_006179.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:49564990 C>G maps to NM_006179.4 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:132016280 G>T maps to NM_001144058.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr11:132180042 C>A maps to NM_001144058.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr11:132177605 G>T maps to NM_001144058.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:2522449 C>T maps to NM_006181.1 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr16:2522768 C>T maps to NM_006181.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:135114557 C>T maps to NM_032536.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:156834540 C>T maps to NM_002529.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:156846358 C>T maps to NM_002529.3 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr1:156846301 G>A maps to NM_002529.3 E581E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:156841431 A>G maps to NM_002529.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr1:156845972 G>T maps to NM_002529.3 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:156845870 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:156834196 G>A maps to NM_002529.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:87338486 G>A did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:88678527 C>T maps to NM_001012338.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr15:88472481 C>T maps to NM_001012338.1 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr15:88679202 A>G maps to NM_001012338.1 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr20:61340678 C>G maps to NM_002531.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr20:61340777 C>T maps to NM_002531.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr20:61341011 C>A maps to NM_002531.2 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr20:61386238 G>C did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:11802342 C>A maps to NM_012344.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:106461044 C>A maps to NM_014840.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:10855684 C>A maps to NM_002484.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:49424478 G>C maps to NM_006184.5 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:49422504 C>T maps to NM_006184.5 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:49409110 C>G maps to NM_006184.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:17333432 G>T maps to ENST00000458064 G259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr8:110287658 T>C maps to NM_032869.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:102894708 C>A maps to NM_031438.2 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:74879865 G>A maps to NM_015901.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:105642974 C>A maps to NM_177533.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr3:131100969 G>A maps to NM_152395.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:145587437 C>T maps to NM_001012758.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr16:56481717 T>A maps to NM_007006.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:63997405 C>T maps to NM_032344.2 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:63997458 C>T maps to NM_032344.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:123843640 G>A maps to NM_007083.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:77769813 C>A maps to NM_001105663.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:71724062 G>A maps to ENST00000393695 R1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:71724414 C>T maps to ENST00000393695 E1384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:71740318 C>A maps to ENST00000393695 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:71724237 C>T maps to ENST00000393695 L1443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:73743957 G>A maps to NM_001005743.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr19:41186908 G>A maps to NM_004756.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:229635457 C>T maps to NM_018230.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:229596516 C>G did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:229631743 C>A maps to NM_018230.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:229599291 G>A maps to NM_018230.2 Q895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:17649456 A>G maps to ENST00000430136 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:17637455 C>A maps to ENST00000430136 E829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr6:17669735 T>A maps to ENST00000430136 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr5:37350301 G>A maps to NM_153485.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:37293024 C>T maps to NM_153485.1 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:37350274 C>A maps to NM_153485.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr5:37299568 C>T maps to NM_153485.1 W1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:47834558 G>A maps to NM_015231.1 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr11:47830024 T>C maps to NM_015231.1 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:47809786 G>C maps to NM_015231.1 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:131760857 C>A maps to NM_015354.1 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr9:131745570 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:131768571 G>A maps to NM_015354.1 A1666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr9:131765729 C>A maps to NM_015354.1 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr7:135307640 C>T maps to NM_015135.2 R1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr7:135287562 C>T maps to NM_015135.2 H841H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:135304535 A>C did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:13395088 C>A maps to NM_024923.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr3:13417072 G>A maps to NM_024923.2 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:13401853 G>A maps to NM_024923.2 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:153984786 G>T maps to NM_207308.2 T1571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:154042812 G>A maps to NM_207308.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:154076575 G>A maps to NM_207308.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:154033013 A>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:154112354 C>A maps to NM_207308.2 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:106411001 G>T did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr23:106410991 G>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr17:73230816 G>A maps to NM_024844.3 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr16:56792531 G>T maps to NM_014669.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr16:56878436 G>A maps to NM_014669.3 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:3727818 C>A maps to NM_016320.4 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr11:3724057 T>C maps to NM_016320.4 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:3794900 A>G maps to NM_016320.4 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr1:224475680 C>T maps to NM_002533.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:224473775 C>A maps to NM_002533.2 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:224475585 G>C maps to NM_002533.2 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:16908678 C>T maps to ENST00000438489 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:16860591 C>G maps to ENST00000438489 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr19:16884027 C>A maps to ENST00000438489 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:62568598 G>T maps to NM_006362.4 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:102335085 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:101096039 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:101095854 T>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:101097734 C>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:101096491 A>C did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:101096498 G>T did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:101096716 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:729315 G>C maps to NM_022463.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:91150624 G>C maps to NM_001161625.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr17:47656016 C>T maps to ENST00000513748 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr12:57619106 G>T maps to NM_007224.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:24878046 C>G maps to NM_025081.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr14:24877619 G>T maps to NM_025081.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:24877434 G>T maps to NM_025081.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:41333967 T>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:41333779 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:41307167 T>A did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:41333812 C>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:41307169 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:120096497 C>T maps to NM_178507.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr12:113435443 A>G maps to NM_016817.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:121465578 G>C maps to NM_003733.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr10:126094045 C>A maps to NM_000274.3 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:105677327 C>A maps to NM_024928.4 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr2:192550415 A>G maps to NM_001031716.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr9:136081732 C>T maps to NM_014581.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:228402726 C>T maps to NM_001098623.1 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:228509745 C>T maps to NM_001098623.1 A5068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:228553853 G>A maps to NM_001098623.1 E6381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:228559482 C>T maps to NM_001098623.1 Q7002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:228475623 C>T maps to NM_001098623.1 F3258F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-39-5031-01A-01D-1441-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:228529139 G>A maps to NM_001098623.1 L5953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:228468289 C>T maps to NM_001098623.1 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:228401978 C>A maps to NM_001098623.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:228480221 A>T did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:228563433 C>A maps to NM_001098623.1 I7565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:228529181 C>T maps to NM_001098623.1 R5967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:228468282 C>T maps to NM_001098623.1 R2661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:228444412 G>A maps to NM_001098623.1 G1457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:220435042 G>C maps to NM_015311.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr8:133044246 C>T maps to ENST00000262283 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:133051284 G>T maps to ENST00000262283 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr8:133044299 C>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr8:133036763 C>G maps to ENST00000262283 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:28096621 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:28116341 C>A maps to NM_000275.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:28202873 C>T maps to NM_000275.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:28273168 G>A maps to NM_000275.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr15:28228541 G>A maps to NM_000275.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr4:48887562 C>A maps to NM_001014446.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:128710349 C>T did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:128696703 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:128692839 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:128709966 C>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:128674793 A>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:128709989 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:128722173 C>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:128723820 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:128722227 C>A did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:128722986 A>G did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:128724197 G>C did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:128709223 G>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:128692882 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:128710039 G>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr2:10582276 C>A maps to NM_002539.1 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:103564204 C>T maps to NM_024410.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr19:463978 T>A maps to NM_182577.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:123518519 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:123805541 C>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:123587185 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:123615584 G>C did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:124030046 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:123538946 G>C did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:123514828 C>G did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:123540169 G>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:123525964 A>G did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:123787590 A>T did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:123839016 C>A did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr23:123775818 A>G did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:123654527 G>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:123870868 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:123518503 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:123870988 C>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:123870952 G>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:123556175 C>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:123516595 G>T did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr23:123514709 C>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:124097471 T>C did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:123515072 C>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:124097424 G>A did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:123514840 A>G did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:123657278 G>C did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:123518272 A>G did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:123615729 G>T did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:123514550 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:123554414 G>T did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:123654450 C>A did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr23:123514790 A>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:124029948 G>C did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:124097478 A>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr5:167645605 C>T maps to NM_001122679.1 V1561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:167630836 G>T maps to NM_001122679.1 G1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr4:183602985 G>C maps to NM_001080477.1 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr4:183713536 C>A maps to NM_001080477.1 T1904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr4:183603015 G>T maps to NM_001080477.1 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr4:183664377 C>A maps to NM_001080477.1 V1145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr4:183575035 T>C maps to NM_001080477.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:183676046 C>T maps to NM_001080477.1 N1509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:78381476 T>A maps to NM_001098816.2 S1971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:13771541 G>A did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr23:13778538 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:13774697 T>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:13771552 G>C did not map to a codon.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr7:44714138 C>A maps to ENST00000444676 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:44737356 G>T maps to ENST00000444676 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr7:44747290 G>T maps to ENST00000444676 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:50954807 G>A maps to NM_018245.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr10:50957774 G>A maps to NM_018245.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr10:50944082 G>T maps to NM_018245.2 R965R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr10:50944483 C>A maps to NM_018245.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr10:50953542 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr10:50952154 T>A maps to NM_018245.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr16:56496444 G>T did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr12:123463862 C>T maps to ENST00000228922 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr12:123463025 G>T maps to ENST00000228922 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr20:61444872 G>T maps to NM_007346.2 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:70784603 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:70777516 G>C did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr10:74684330 G>A maps to NM_152635.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:174987918 C>T maps to ENST00000409546 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr10:15107716 C>T maps to NM_018324.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:137967605 C>T maps to NM_014279.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:9965212 G>A maps to NM_058164.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:9965170 C>T maps to NM_058164.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:102290774 G>T maps to ENST00000338858 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:102270308 G>A maps to ENST00000338858 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:161967614 C>A maps to ENST00000451379 G493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:161976197 G>T maps to ENST00000451379 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr15:53081522 G>A maps to NM_004498.1 L187L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-66-2800-01A-01D-1267-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:74079479 C>A maps to NM_001080507.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:193349399 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:193372725 G>T maps to NM_130837.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:193349412 G>T maps to NM_130837.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:46087919 C>A maps to NM_001017989.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:132398958 G>T maps to NM_002545.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr11:132307139 G>T maps to NM_002545.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:67283826 C>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:67432045 G>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:67283738 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:67316831 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:67454366 G>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:67652752 T>C did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr8:145106850 G>A maps to ENST00000360660 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:153416410 C>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:153418502 A>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:153416361 C>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:153416371 C>G did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr7:128412599 G>C maps to NM_001708.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:128415661 G>T maps to NM_001708.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr7:128415784 C>T maps to NM_001708.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:241757786 G>A maps to NM_014322.2 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:241767864 G>C maps to NM_014322.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:88423457 C>T maps to NM_001030015.2 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr6:47754338 C>T maps to ENST00000489301 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:47779407 A>G did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr6:47775993 C>A maps to ENST00000489301 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:54142384 G>A maps to NM_000912.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr8:54142276 G>A maps to NM_000912.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr8:54142387 G>A maps to NM_000912.3 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr20:62724186 C>G maps to NM_000913.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:154360939 A>C maps to NM_001145279.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:203472826 C>A maps to NM_014359.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:6891164 C>T maps to NM_001004460.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:6891617 C>A maps to NM_001004460.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr11:7960134 T>C maps to NM_001003745.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr11:6898393 C>A maps to NM_207186.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr12:55615656 T>A maps to NM_001005280.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:55614954 C>A maps to NM_001005280.1 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:55735765 G>A maps to NM_001005491.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:55735342 C>T maps to NM_001005491.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr11:55735360 T>A maps to NM_001005491.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr11:55735330 C>T maps to NM_001005491.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr6:29407983 C>A maps to NM_013941.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr14:22038005 A>G maps to NM_001005465.1 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr11:123886785 G>T maps to NM_001004462.1 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr11:123886703 C>A maps to NM_001004462.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:123909462 G>A maps to NM_001004463.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:123909600 A>G maps to NM_001004463.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:123909585 G>A maps to NM_001004463.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:123900903 C>A maps to ENST00000375021 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:123900598 T>C maps to NM_001004464.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:123900522 C>A maps to NM_001004464.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr11:123893736 C>G maps to NM_001001953.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr11:123893757 G>T maps to NM_001001953.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:123894396 G>T maps to NM_001001953.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr11:123894282 T>A maps to NM_001001953.1 C188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:123893841 C>T maps to NM_001001953.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr19:15918066 G>A maps to NM_013940.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:15918196 G>T maps to NM_013940.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr19:15839194 G>T maps to NM_013939.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:15839698 C>A maps to NM_013939.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr19:15852339 C>T maps to NM_013938.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:16060371 C>T maps to NM_001004465.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:15905715 C>A maps to NM_001004466.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:159410498 G>T maps to NM_012351.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:159409848 C>T maps to NM_012351.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:159283909 A>T maps to NM_001004467.1 C180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:159505092 C>T maps to NM_001004469.1 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:158435623 C>A maps to NM_001004473.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:158390311 C>T maps to NM_001004476.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:158389819 A>G maps to NM_001004476.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:57995795 G>T maps to NM_001004471.2 C184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:57995615 G>T maps to NM_001004471.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:57995828 G>A maps to NM_001004471.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:158449909 C>T maps to NM_001004472.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr11:123847929 C>A maps to NM_001004474.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:123847780 G>T maps to NM_001004474.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:123847650 G>T maps to NM_001004474.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:158368475 G>T maps to NM_001004475.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:158369187 C>T maps to NM_001004475.1 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr11:58034970 C>T maps to NM_207374.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:58034691 C>T maps to NM_207374.3 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:58034511 G>T maps to NM_207374.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:158549011 G>T maps to NM_001004477.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr1:158549353 A>T maps to NM_001004477.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:158576473 C>A maps to NM_001004478.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr14:20666363 C>A maps to NM_001005503.1 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:20665547 T>C maps to NM_001005503.1 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr14:19377712 C>A maps to NM_001013354.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:19377712 C>A maps to NM_001013354.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:19378027 G>A maps to NM_001013354.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr14:20711714 G>A maps to NM_001004479.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr14:20692524 C>T maps to NM_001004480.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:20692743 C>A maps to NM_001004480.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:248004561 G>A maps to NM_001001959.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr1:248005144 C>T maps to NM_001001959.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:248004823 G>T maps to NM_001001959.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:248004841 G>T maps to NM_001001959.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:29364841 G>T maps to NM_013936.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr6:29365009 T>C maps to NM_013936.3 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr10:45799861 C>A maps to NM_001004297.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:45799723 G>A maps to NM_001004297.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr9:107289088 G>A maps to NM_001001919.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:107361116 G>C maps to NM_001004482.1 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr9:107379750 C>A maps to NM_001001956.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:107457199 C>A maps to NM_001004484.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr9:107266755 C>A maps to NM_001004485.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr9:107266677 G>T maps to NM_001004485.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr1:247836256 G>T maps to NM_001005487.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:247835986 G>C maps to NM_001005487.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:247835992 A>C maps to NM_001005487.1 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:130678729 G>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:35870089 C>T maps to NM_001004487.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:247978806 C>A maps to NM_001001966.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr1:247978179 G>C maps to NM_001001966.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:248845392 G>T maps to NM_001004734.1 Y71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:248845377 C>A maps to NM_001004734.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:248844999 T>C maps to NM_001004734.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:3118955 C>A maps to NM_014565.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:3119288 C>A maps to NM_014565.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr17:3101462 T>C maps to NM_012352.1 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:247920934 G>C maps to NM_012353.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:247920943 G>T maps to NM_012353.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:247921567 C>T maps to NM_012353.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:2996074 G>A maps to NM_002548.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr17:2996152 G>A maps to NM_002548.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr17:2995591 C>T maps to NM_002548.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr17:3336247 G>T maps to NM_003554.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:3254962 C>T maps to NM_012360.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr16:3254527 C>T maps to NM_012360.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:125563090 C>A maps to NM_080859.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr9:125487158 T>C maps to NM_001005235.1 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:125486621 T>C maps to NM_001005235.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr9:125486387 G>A maps to NM_001005235.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr9:125486936 C>A maps to NM_001005235.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:9204663 T>C maps to ENST00000305465 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:9204717 C>T maps to ENST00000305465 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr9:125316420 G>T maps to NM_001004457.1 G325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:57982932 G>C maps to NM_001004458.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:57982686 C>T maps to NM_001004458.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:57971605 T>C maps to NM_001004459.1 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:57970846 T>C maps to NM_001004459.1 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr7:144015480 C>A maps to NM_001005287.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr7:143793121 A>C maps to NM_001004135.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:143792421 G>A maps to NM_001004135.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:143826660 C>T maps to NM_001001659.1 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:143826538 C>T maps to NM_001001659.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:143807314 C>T maps to NM_001005480.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr7:143807526 G>T maps to NM_001005480.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:143806806 C>A maps to NM_001005480.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:143771941 C>T maps to NM_001004488.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr7:143771728 C>T maps to NM_001004488.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr7:143771479 C>A maps to NM_001004488.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr7:143747997 C>T maps to NM_012365.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:6806906 T>A maps to NM_001004489.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr11:6806969 G>A maps to NM_001004489.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:248129571 G>T maps to NM_001004491.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:248129374 G>T maps to NM_001004491.1 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:247614642 G>C maps to NM_001004492.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr1:247614351 C>T maps to NM_001004492.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:247614884 G>A maps to NM_001004492.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr6:27879590 A>G maps to NM_033057.2 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:27879782 C>A maps to NM_033057.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr6:27879970 G>A maps to NM_033057.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr6:29054113 C>A maps to NM_001005226.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr6:29054566 G>A maps to NM_001005226.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:29054911 G>C maps to NM_001005226.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:29054190 C>A maps to NM_001005226.2 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr6:27925263 A>T maps to NM_012367.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr6:27925953 G>A maps to NM_012367.1 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr6:27925239 C>G maps to NM_012367.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr6:27925356 T>C maps to NM_012367.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:247694936 G>A maps to NM_198074.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:247695726 G>A maps to NM_198074.4 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:247695000 C>T maps to NM_198074.4 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:247695264 G>T maps to NM_198074.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:6942354 C>A maps to NM_001004684.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:143657641 C>T maps to NM_012369.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr7:143657677 T>C maps to NM_012369.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:143632562 C>T maps to NM_001004685.1 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:247752440 C>T maps to NM_001001915.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr1:247752239 G>T maps to NM_001001915.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:247752410 G>A maps to NM_001001915.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:247752206 C>T maps to NM_001001915.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:247752338 C>T maps to NM_001001915.1 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr1:247769663 C>A maps to NM_001001914.1 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:247769105 C>T maps to NM_001001914.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:247769575 C>A maps to NM_001001914.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:247769301 C>A maps to NM_001001914.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:247769168 C>T maps to NM_001001914.1 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:247769288 C>A maps to NM_001001914.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:247769803 C>A maps to NM_001001914.1 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:248685324 C>T maps to NM_001013355.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:248685249 C>G maps to NM_001013355.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:248685820 C>T maps to NM_001013355.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr6:29141952 G>T maps to NM_030905.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr9:114089855 G>A maps to ENST00000374428 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:248262937 C>A maps to NM_175911.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:248262724 G>T maps to NM_175911.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:248263519 C>A maps to NM_175911.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:248202132 C>T maps to NM_001004686.2 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:248202387 G>T maps to NM_001004686.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:248201673 A>T maps to NM_001004686.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:248202063 C>A maps to NM_001004686.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248224129 C>T maps to NM_001004687.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248224426 G>A maps to NM_001004687.1 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr1:248224405 G>T maps to NM_001004687.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:248224063 C>T maps to NM_001004687.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:248224438 G>T maps to NM_001004687.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248112239 C>T maps to NM_001001963.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:248112245 C>G maps to NM_001001963.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:248343730 C>T maps to NM_001004688.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:248343427 C>T maps to NM_001004688.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr1:248343382 G>C maps to NM_001004688.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:248344135 C>T maps to NM_001004688.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:248344162 C>T maps to NM_001004688.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:248343550 C>A maps to NM_001004688.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:248344096 G>A maps to NM_001004688.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:248367124 T>A maps to NM_001004689.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:248366572 C>T maps to NM_001004689.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:248366464 G>C maps to NM_001004689.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:248402871 C>A maps to NM_017504.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:248308529 C>T maps to NM_001004690.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:248308991 C>T maps to NM_001004690.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:248309294 T>C maps to NM_001004690.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:248487633 G>T maps to NM_001004691.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:248569699 C>A maps to NM_030904.1 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:248569753 C>G maps to NM_030904.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:248569618 C>A maps to NM_030904.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:248570188 G>A maps to NM_030904.1 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:248569834 G>T maps to NM_030904.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:248569945 C>T maps to NM_030904.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248789646 G>A maps to NM_001001964.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248789952 G>A maps to NM_001001964.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:248790216 G>T maps to NM_001001964.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:248458693 G>A maps to NM_001004692.1 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248616385 G>A maps to NM_001004136.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:248814023 G>A maps to NM_001001824.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr1:248813459 G>A maps to NM_001001824.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:248722768 G>A maps to ENST00000328570 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:248636959 G>T maps to NM_001005495.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:248637585 C>A maps to NM_001005495.1 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248436732 G>A maps to NM_001004695.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:248436846 G>T maps to NM_001004695.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:248436831 A>G maps to NM_001004695.1 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:248436605 C>A maps to NM_001004695.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:248737428 G>T maps to NM_001001821.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:248737518 C>A maps to NM_001001821.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr1:248737724 G>A maps to NM_001001821.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:248737467 G>C maps to NM_001001821.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:248801899 G>A maps to NM_001001827.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248525367 C>T maps to NM_001004696.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:248524898 G>A maps to NM_001004696.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:248525823 T>A maps to NM_001004696.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:248525428 C>T maps to NM_001004696.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:248525718 G>T maps to NM_001004696.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:248525259 C>T maps to NM_001004696.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:248525904 T>A maps to NM_001004696.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:248525460 C>A maps to NM_001004696.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:248525697 C>A maps to NM_001004696.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:248550956 G>T maps to NM_001005471.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:248551325 G>T maps to NM_001005471.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:248551172 C>A maps to NM_001005471.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr6:29012352 G>A maps to NM_030903.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr6:29012693 C>A maps to NM_030903.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:248058950 C>T maps to NM_001001957.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:248059310 C>A maps to NM_001001957.2 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:248059181 C>T maps to NM_001001957.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:248059541 C>G maps to NM_001001957.2 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:248058998 G>T maps to NM_001001957.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:248059532 G>C maps to NM_001001957.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:247654713 C>T maps to NM_001004698.2 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:247655289 C>A maps to NM_001004698.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:247654486 C>A maps to NM_001004698.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:247655151 G>C maps to NM_001004698.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:247655380 G>T maps to NM_001004698.2 G318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:180166857 G>A maps to NM_001001657.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:180166563 G>T maps to NM_001001657.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr17:3195411 A>G maps to ENST00000397187 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr17:3195188 G>T maps to ENST00000397187 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:3195369 G>C maps to ENST00000397187 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:3195693 G>T maps to ENST00000397187 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr17:3181485 G>T maps to NM_002551.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:55135841 G>A maps to NM_001005275.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:55136360 A>C maps to NM_001005275.1 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:55135382 C>T maps to NM_001005275.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:55135857 C>A maps to NM_001005275.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:55136372 G>A maps to NM_001005275.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:55111341 C>T maps to NM_001005274.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:55111020 G>T maps to NM_001005274.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:55111056 G>C maps to NM_001005274.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:48511132 C>T maps to NM_001005512.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:48510769 G>C maps to NM_001005512.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr11:48510835 C>A maps to NM_001005512.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:48510826 T>C maps to NM_001005512.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:51411576 G>C maps to NM_001005272.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:51411540 C>G maps to NM_001005272.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:51412239 G>A maps to NM_001005272.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr11:48238462 T>C maps to NM_001005470.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:48239092 G>C maps to NM_001005470.1 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr11:55371720 A>T maps to NM_001004700.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:50003962 C>A maps to NM_001005270.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:50003422 G>T maps to NM_001005270.2 C205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:50003188 C>G maps to NM_001005270.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:50003788 G>T maps to NM_001005270.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr11:49974693 C>A maps to NM_001001955.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:49974873 T>A maps to NM_001001955.2 C300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr11:49974138 C>A maps to NM_001001955.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr11:55322711 A>G maps to NM_001001920.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr11:55322396 C>A maps to NM_001001920.1 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:55322666 T>A maps to NM_001001920.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:55339799 T>A maps to NM_001004701.2 L66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:55340085 C>A maps to NM_001004701.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:55340460 G>T maps to NM_001004701.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:48346767 C>T maps to NM_001004702.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr11:48347190 G>T maps to NM_001004702.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:48347277 C>G maps to NM_001004702.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:51515730 C>T maps to NM_001004703.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:51515877 C>G maps to NM_001004703.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:51515760 C>T maps to NM_001004703.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:51515298 C>T maps to NM_001004703.1 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:51515934 C>A maps to NM_001004703.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:55433436 A>T maps to NM_001004704.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:55433451 T>A maps to NM_001004704.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:55433292 G>T maps to NM_001004704.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr11:55432932 C>A maps to NM_001004704.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:55433569 T>A maps to NM_001004704.1 *310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:55433052 G>T maps to NM_001004704.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr11:55432842 G>A maps to NM_001004704.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr11:55432896 C>G maps to NM_001004704.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:55432848 C>A maps to NM_001004704.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:56232860 C>G maps to NM_012374.1 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:59245657 G>A maps to NM_001004705.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:59245474 C>T maps to NM_001004705.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:56247069 G>A maps to NM_001004707.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr17:56247783 C>T maps to NM_001004707.3 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:123810487 G>T maps to NM_001001965.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr11:123811093 C>A maps to NM_001001965.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:123810586 C>T maps to NM_001001965.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:59224894 G>A maps to NM_001004708.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr11:59224642 C>T maps to NM_001004708.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:59282786 C>G maps to NM_001004711.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr15:102358598 T>C maps to NM_001001674.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:102346095 C>T maps to NM_001005326.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr15:102346038 G>T maps to NM_001005326.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr15:102346434 T>C maps to NM_001005326.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr15:102346590 G>T maps to NM_001005326.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:20404460 G>C maps to NM_001004063.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr14:20404280 C>T maps to NM_001004063.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:20483070 G>A maps to NM_001004712.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr14:20483022 C>A maps to NM_001004712.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:20482683 G>T maps to NM_001004712.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr14:20482707 G>C maps to NM_001004712.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr14:20483160 C>A maps to NM_001004712.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr14:20443958 C>T maps to NM_001005486.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr14:20444237 T>C maps to NM_001005486.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:20444090 C>T maps to NM_001005486.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr14:20444144 C>A maps to NM_001005486.1 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr14:20444612 G>C maps to NM_001005486.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr14:20586278 C>T maps to NM_001004715.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr14:20389652 T>A maps to NM_001005483.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:20389541 G>A maps to NM_001005483.1 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr14:20389499 A>G maps to NM_001005483.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr14:20389095 G>T maps to NM_001005483.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr14:20388875 C>A maps to NM_001005483.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr14:20389169 C>A maps to NM_001005483.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr14:20528916 C>A maps to NM_001004717.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr14:20528226 A>G maps to NM_001004717.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr14:20248789 C>T maps to NM_001005500.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr14:20249407 G>A maps to NM_001005500.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr14:20249277 C>A maps to NM_001005500.1 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:20249221 C>A maps to NM_001005500.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr14:20249063 G>T maps to NM_001005500.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr15:22369096 A>G maps to NM_001004719.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr15:22369130 C>A maps to NM_001004719.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr15:22369505 A>T maps to NM_001004719.2 K311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr14:20295819 A>G maps to NM_001004723.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:20295660 C>T maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr14:20295780 C>A maps to NM_001004723.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr15:22383114 C>T maps to NM_001005241.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:22382510 C>A maps to NM_001005241.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:20612187 C>T maps to NM_001004724.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:20612100 G>T maps to NM_001004724.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr14:20612367 A>T maps to NM_001004724.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr14:20612463 C>A maps to NM_001004724.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr11:55406375 T>C maps to NM_001004124.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:55406051 C>A maps to NM_001004124.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:55406498 C>A maps to NM_001004124.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr11:55406750 G>A maps to NM_001004124.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr14:20216260 C>A maps to NM_172194.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr14:20216179 G>T maps to NM_172194.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:48328070 C>G maps to NM_001004725.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:48328448 C>T maps to NM_001004725.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:55418600 C>G maps to NM_001004059.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr11:55418885 C>T maps to NM_001004059.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr11:55419063 G>T maps to NM_001004059.2 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:55418579 G>T maps to NM_001004059.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:48285558 C>A maps to NM_001004726.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:48286056 C>A maps to NM_001004726.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr11:48267362 C>T maps to NM_001004727.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:48266675 G>T maps to NM_001004727.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:48266730 T>C maps to NM_001004727.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:4976472 C>T maps to NM_001004748.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:4967859 C>T maps to NM_001005329.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr11:4967982 G>T maps to NM_001005329.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr11:4967667 C>G maps to NM_001005329.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:4968318 G>T maps to NM_001005329.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:4967562 G>T maps to NM_001005329.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr11:4967583 C>G maps to NM_001005329.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:5322672 G>T maps to NM_033179.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:5373579 C>T maps to NM_001004750.1 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr11:5373351 C>G maps to NM_001004750.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr11:4661499 T>A maps to NM_001004751.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:4790941 G>T maps to ENST00000380383 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:4790943 T>C maps to ENST00000380383 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:4936659 G>A maps to NM_001005238.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:4936227 A>T maps to NM_001005238.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:5462288 G>T maps to NM_001005288.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr11:5462446 G>A maps to NM_001005288.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:5461846 C>A maps to NM_001005288.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:5474865 C>A maps to NM_001004754.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:5475617 C>A maps to NM_001004754.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr11:5020859 A>T maps to NM_001004755.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr11:5020319 A>G maps to NM_001004755.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:5410987 C>T maps to NM_001004756.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr11:5411215 G>C maps to NM_001004756.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:5411035 G>T maps to NM_001004756.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:5410896 T>A maps to NM_001004756.2 L90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr11:4869505 G>C maps to NM_001004758.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:4903905 C>T maps to NM_001004759.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr11:4903506 G>A maps to NM_001004759.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:4903563 G>A maps to NM_001004759.1 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr11:4903251 C>G maps to NM_001004759.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:4903113 G>A maps to NM_001004759.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr11:5221785 A>G maps to NM_001004760.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:5142491 C>T maps to NM_001005222.2 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:5142211 A>G maps to NM_001005222.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:5142453 G>A maps to NM_001005222.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:5142712 C>T maps to NM_001005222.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr11:5153674 G>T maps to NM_001005160.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:5153745 C>A maps to NM_001005160.2 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:5153380 G>T maps to NM_001005160.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr11:6190815 G>A maps to NM_001004052.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:6190632 C>A maps to NM_001004052.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr11:6191057 G>T maps to NM_001004052.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:6191169 A>G maps to NM_001004052.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:6190908 G>T maps to NM_001004052.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr11:6191106 G>A maps to NM_001004052.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:4389099 C>A maps to NM_001005161.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:4389417 G>C maps to NM_001005161.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:5906037 G>T maps to NM_001005165.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:5863043 C>T maps to ENST00000379946 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:5862857 A>G maps to ENST00000379946 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:5862212 C>T maps to ENST00000379946 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr11:5878629 T>A maps to NM_001005168.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:5566078 G>T maps to NM_001005289.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr11:5566078 G>C maps to NM_001005289.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:4615723 C>T maps to ENST00000450052 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:4608327 C>T maps to NM_001005170.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:4608224 G>T maps to NM_001005170.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:4608294 C>A maps to NM_001005170.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:5068594 C>A maps to NM_001001916.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:4510282 C>A maps to NM_001005171.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:4470670 C>T maps to NM_001005172.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:6007815 G>T maps to NM_001005173.2 C115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:4567166 T>A maps to NM_001004137.1 C249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:5809635 G>A maps to NM_001001913.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr11:5809818 G>T maps to NM_001001913.1 C76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:5809644 A>T maps to NM_001001913.1 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:5842194 G>T maps to NM_001005174.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:5842404 C>A maps to NM_001005174.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr11:5776677 G>A maps to NM_001005175.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:5799006 C>A maps to NM_001001922.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr11:5799597 A>G maps to NM_001001922.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr11:5798964 A>T maps to NM_001001922.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:4825571 C>A maps to ENST00000380382 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:6221262 T>C maps to NM_001005178.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:6048178 G>A maps to NM_001001917.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr11:6048127 G>A maps to NM_001001917.2 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:5968750 C>T maps to NM_001003443.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:5969055 T>A maps to NM_001003443.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:5969289 G>T maps to NM_001003443.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr11:5968710 C>G maps to NM_001003443.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:5969254 C>T maps to NM_001003443.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:5969376 G>T maps to NM_001003443.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:5969163 C>T maps to NM_001003443.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr11:5969274 G>A maps to NM_001003443.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:6023925 G>T maps to NM_001005179.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:6023985 G>C maps to NM_001005179.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr11:5758096 G>T maps to NM_001005180.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr11:5758306 G>T maps to NM_001005180.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr11:6129307 C>A maps to NM_001005181.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:59211430 C>T maps to NM_001004728.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:59211285 C>G maps to NM_001004728.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:59211378 G>A maps to NM_001004728.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:97806129 C>G maps to NM_054106.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:56409732 G>A maps to NM_001002925.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:56409759 A>T maps to NM_001002925.1 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:55798322 C>A maps to NM_001001921.1 C143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:21623337 G>A maps to NM_001004731.1 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr14:21623455 G>C maps to NM_001004731.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr11:58206754 C>G maps to NM_001004733.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr11:58207459 G>T maps to NM_001004733.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:58207150 A>T maps to NM_001004733.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:58207078 G>A maps to NM_001004733.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:58190359 G>A maps to NM_001005566.2 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr11:58190569 G>T maps to NM_001005566.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:58189969 G>A maps to NM_001005566.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:58190173 G>A maps to NM_001005566.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:58190239 A>C maps to NM_001005566.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:58274945 G>T maps to NM_001005218.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr11:58170405 C>A maps to NM_001005469.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:58170462 A>T maps to NM_001005469.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:55541797 G>A maps to NM_001001967.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr11:55541395 C>A maps to NM_001001967.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:55541386 C>A maps to NM_001001967.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr11:55541773 G>T maps to NM_001001967.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:55541449 T>C maps to NM_001001967.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:55541233 C>A maps to NM_001001967.1 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:55563066 C>A maps to NM_001004735.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr11:55563597 G>T maps to NM_001004735.1 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:55563672 G>C maps to NM_001004735.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:55607000 C>A maps to NM_001005496.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:55606814 C>T maps to NM_001005496.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:55606494 G>T maps to NM_001005496.1 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr11:55606580 G>T maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:55587662 C>T maps to ENST00000395203 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:55587701 G>T maps to ENST00000395203 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr11:55587890 G>T maps to ENST00000395203 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:55587836 C>T maps to ENST00000395203 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr11:55587446 T>C maps to ENST00000395203 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:55587509 T>C maps to ENST00000395203 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:55587160 C>A maps to ENST00000395203 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:55587800 C>G maps to ENST00000395203 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:55761501 A>T maps to NM_003697.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr11:55761489 A>T maps to NM_003697.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:55761942 G>C maps to NM_003697.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:55761941 G>A maps to NM_003697.1 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:55761777 C>T maps to NM_003697.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:55761639 C>T maps to NM_003697.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:97852475 C>G maps to NM_001005338.1 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:97868732 C>T maps to NM_001005514.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr3:97868651 C>T maps to NM_001005514.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr3:97887995 T>G maps to NM_001005515.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:98002462 C>A maps to NM_001005482.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr3:98002675 G>C maps to NM_001005482.1 *315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:97983679 C>T maps to NM_001005479.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:97984102 T>A maps to NM_001005479.1 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr3:97983259 C>T maps to NM_001005479.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:97983217 C>T maps to NM_001005479.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:97983943 C>A maps to NM_001005479.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:97983198 T>A maps to NM_001005479.1 L24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:55703453 G>T maps to NM_006637.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:55703747 C>T maps to NM_006637.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr11:55703273 G>T maps to NM_006637.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:55703273 G>T maps to NM_006637.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr11:55944866 C>T maps to NM_001005492.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr11:55944432 T>C maps to NM_001005492.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:55945004 C>A maps to NM_001005492.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:55944668 C>T maps to NM_001005492.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:98072900 G>C maps to NM_001005517.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr11:55579640 C>A maps to NM_001004738.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:55579265 G>T maps to NM_001004738.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:55579832 G>T maps to NM_001004738.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:55594909 C>A maps to NM_001004739.1 C72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:55595416 T>C maps to NM_001004739.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:56380723 G>A maps to NM_001004740.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:56380540 A>G maps to NM_001004740.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:56380692 C>A maps to NM_001004740.1 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:56380582 G>A maps to NM_001004740.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:56344384 G>A maps to NM_001004741.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:56310526 C>A maps to NM_001005245.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:56237922 G>A maps to NM_001004742.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:56258003 G>A maps to NM_001005282.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:56258234 C>T maps to NM_001005282.1 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr11:56258189 G>T maps to NM_001005282.1 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr11:56258429 C>A maps to NM_001005282.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:7817697 A>T maps to NM_153444.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:7818156 C>A maps to NM_153444.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr11:56184865 C>T maps to NM_001004744.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr11:56184913 A>G maps to NM_001004744.1 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:56185405 C>A maps to NM_001004744.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:56043842 T>A maps to NM_001004745.1 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:56043881 C>T maps to NM_001004745.1 H256H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:56043398 C>A maps to NM_001004745.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr11:56000487 G>A maps to NM_001004746.1 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:56000265 T>A maps to NM_001004746.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:56000523 A>G maps to NM_001004746.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:56020019 C>T maps to NM_001004747.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr11:56019794 C>A maps to NM_001004747.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:29323093 C>T maps to NM_030876.5 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr6:29323507 G>A maps to NM_030876.5 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:55681455 G>T maps to NM_001001960.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:55681782 T>A maps to NM_001001960.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr11:55681827 A>T maps to NM_001001960.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:6816426 G>T maps to NM_003696.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr7:143701562 G>A maps to NM_001005281.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr7:143701538 C>A maps to NM_001005281.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:143701706 C>T maps to NM_001005281.1 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr7:143701478 C>A maps to NM_001005281.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:240969638 C>A maps to NM_001005853.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:240968954 T>A maps to NM_001005853.1 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:240984556 G>T maps to NM_173351.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:55715294 G>A maps to NM_001005182.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr12:55715174 T>C maps to NM_001005182.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:55714514 C>A maps to NM_001005182.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:55846128 C>T maps to NM_054105.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:55794479 T>A maps to NM_001005518.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:55641499 C>T maps to NM_001005490.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr12:55641479 A>T maps to NM_001005490.1 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:55820348 T>C maps to NM_001005183.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:247875682 G>A maps to NM_001005286.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:247875889 A>G maps to NM_001005286.1 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:158669892 G>A maps to NM_001005279.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:158669553 C>A maps to NM_001005279.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:158724841 G>T maps to NM_001005184.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:123676934 G>T maps to NM_001005325.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr11:123676136 G>T maps to NM_001005325.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:158736076 G>T maps to NM_001005185.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:158735719 G>A maps to NM_001005185.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:158736094 G>A maps to NM_001005185.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:158747221 G>A maps to NM_001005278.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr11:57799185 C>A maps to NM_001005186.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr11:57799281 G>C maps to NM_001005186.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr14:21109187 G>T maps to NM_001001968.1 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:123814149 A>G maps to NM_001005187.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr11:123624809 G>T maps to NM_001005188.1 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:158517430 G>A maps to NM_001005189.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:14952020 G>A maps to NM_001005190.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:14952632 C>T maps to NM_001005190.1 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr19:14991870 G>T maps to NM_030901.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:15053202 G>A maps to NM_012377.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:9213754 G>T maps to NM_001005193.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:9213748 G>T maps to NM_001005193.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:9236951 G>A maps to NM_001001958.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:124440848 C>A maps to NM_001005194.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr11:124440461 C>T maps to NM_001005194.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:124440878 C>A maps to NM_001005194.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:124440530 C>G maps to NM_001005194.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:124440626 C>T maps to NM_001005194.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:124440188 C>G maps to NM_001005194.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:124413055 C>T maps to NM_001005195.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:124413504 A>G maps to NM_001005195.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:124412887 G>T maps to NM_001005195.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:124252600 G>T maps to NM_001005468.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:124252378 G>A maps to NM_001005468.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:124252312 C>T maps to NM_001005468.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr11:124294665 G>T maps to NM_001005196.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:124294593 G>T maps to NM_001005196.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:124294656 G>A maps to NM_001005196.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr11:124294350 G>T maps to NM_001005196.1 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:124310854 G>A maps to NM_012378.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:124310357 A>G maps to NM_012378.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr11:124189346 G>T maps to NM_001002918.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:124189229 T>A maps to NM_001002918.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:124189673 G>T maps to NM_001002918.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr11:124189985 C>G maps to NM_001002918.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:123777854 C>T maps to NM_001005197.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:123777641 C>T maps to NM_001005197.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:124095816 C>A maps to NM_001007249.1 C140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:56057655 C>A maps to NM_001005199.1 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr11:56058338 G>T maps to NM_001005199.1 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:56057842 T>C maps to NM_001005199.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:55872535 T>C maps to NM_001005200.1 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr11:55872907 A>G maps to NM_001005200.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:55873109 C>T maps to NM_001005200.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:55890050 C>A maps to NM_001005201.1 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr11:55890375 C>T maps to NM_001005201.1 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:55890504 G>A maps to NM_001005201.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr11:55890081 C>T maps to NM_001005201.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:55890144 C>A maps to NM_001005201.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:55861586 C>T maps to NM_001003750.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:55861616 G>A maps to NM_001003750.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:55861249 C>A maps to NM_001003750.1 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:55861448 A>T maps to NM_001003750.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:55861586 C>A maps to NM_001003750.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:55861451 C>A maps to NM_001003750.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr11:55861579 C>A maps to NM_001003750.1 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:56127805 C>T maps to NM_001005205.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:56128354 G>A maps to NM_001005205.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:55904849 C>A maps to NM_001004064.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr11:55904849 C>T maps to NM_001004064.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr11:55904843 C>A maps to NM_001004064.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:55904297 A>G maps to NM_001004064.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:56113717 C>T maps to NM_001002907.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:56113633 A>T maps to NM_001002907.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:56086191 C>A maps to NM_001005202.1 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:55927224 G>C maps to NM_001004058.2 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:55927655 G>A maps to NM_001004058.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr11:55927466 G>T maps to NM_001004058.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:48919788 C>T maps to NM_001005203.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:142723948 G>A maps to NM_001001658.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:142723505 G>A maps to NM_001001658.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:142723685 C>G maps to NM_001001658.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:56468291 G>A maps to NM_001013358.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:56468237 C>A maps to NM_001013358.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:56468597 C>A maps to NM_001013358.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr11:56468291 G>T maps to NM_001013358.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:56510795 G>A maps to NM_001005284.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr11:56511194 A>T maps to NM_001005284.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:56510513 G>T maps to NM_001005284.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:57886367 G>T maps to NM_001005211.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr11:57886592 T>A maps to NM_001005211.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:57886013 G>A maps to NM_001005211.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:55524229 C>T maps to NM_001005243.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:57947062 C>A maps to NM_001005212.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:57958291 C>A maps to NM_001005283.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:57958003 T>C maps to NM_001005283.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr11:57958306 G>T maps to NM_001005283.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:122079194 G>A maps to NM_032790.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:102087216 C>T maps to NM_032831.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:201796150 C>T maps to NM_006190.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:88311520 G>T maps to NM_181837.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:148705763 C>T maps to NM_181742.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr7:103824481 C>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:103808924 C>T maps to NM_002553.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:31302238 G>A maps to NM_030758.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:31725156 G>C maps to NM_017784.4 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:125266341 C>A maps to NM_022776.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:125257329 C>T maps to NM_022776.4 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:125286248 G>T maps to NM_022776.4 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:21892061 C>A maps to NM_080597.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr18:21758026 C>T maps to NM_080597.2 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr18:21957470 A>T maps to NM_080597.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr18:21913047 G>A maps to NM_080597.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr20:60835155 C>T maps to NM_144498.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr20:60856155 C>A maps to NM_144498.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr7:24854818 A>G maps to NM_015550.2 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr11:3114760 C>A maps to NM_020896.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr2:179236929 C>T maps to ENST00000392505 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:179236960 G>T did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr2:179201134 G>T maps to ENST00000392505 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:179259109 C>A maps to ENST00000392505 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:76767174 T>A maps to NM_020841.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:20916905 G>A maps to NM_017807.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr16:83999365 C>T maps to NM_013370.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:30659937 C>A maps to NM_020530.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:38881756 C>T maps to NM_003999.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:38919141 C>A maps to NM_003999.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:38932054 G>A maps to NM_003999.2 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr5:38931985 C>T maps to NM_003999.2 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:38921867 C>T maps to NM_003999.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:19553398 C>G maps to NM_145260.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr2:19552083 C>G maps to NM_145260.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:99963889 G>C maps to ENST00000457907 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr8:99961746 C>A maps to ENST00000457907 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr3:195954569 C>T maps to NM_152672.5 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:38229090 G>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:38226643 T>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:38268030 G>A did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr16:21702907 T>A maps to ENST00000286149 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:21721273 G>A maps to ENST00000286149 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:21693106 G>C maps to ENST00000286149 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:26706344 G>A maps to NM_194248.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:26684723 C>T maps to NM_194248.2 W1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:26696416 G>T maps to NM_194248.2 R1143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:26717815 G>C maps to NM_194248.2 Y297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:161214690 G>A maps to NM_001080440.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr4:4228189 G>T maps to NM_177998.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72929486 C>T maps to NM_178160.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr5:76932927 G>T maps to NM_032109.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:76932786 C>T maps to NM_032109.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:48801471 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:69282923 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:69283240 G>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:31776858 C>A maps to ENST00000382902 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr2:63282958 G>C maps to NM_014562.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:63283219 C>T maps to NM_014562.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr12:29617470 A>G maps to NM_183378.2 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:29628066 C>A maps to NM_183378.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:29631787 G>C maps to NM_183378.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:29639210 T>C maps to NM_183378.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:29639177 C>G did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:111966323 G>T maps to ENST00000369728 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:111957654 C>A maps to ENST00000369728 G554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:23235849 C>T maps to NM_005015.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr13:97639158 G>A maps to NM_080818.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr3:16327950 C>T maps to NM_138381.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr3:25832948 T>A maps to NM_017897.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:38271888 A>T maps to NM_005109.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:3807226 G>T maps to NM_002558.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr12:133197897 C>A maps to NM_170683.2 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:57106059 C>A maps to NM_002559.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:57114587 A>G did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr12:121666569 G>A maps to NM_002560.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:152553672 C>T maps to NM_002563.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:78216989 C>A did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:78216994 C>T did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:78216920 C>G did not map to a codon.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr23:78216452 C>G did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:78216934 C>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:78216167 G>T did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:78216656 A>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:151056471 C>G maps to NM_022788.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr3:151046126 A>G maps to NM_176894.2 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:150931183 A>T maps to NM_014879.3 C307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:72945944 C>T maps to NM_176071.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:69478396 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:73007626 G>T maps to NM_004154.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:1584629 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:1585300 G>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:1584848 C>A did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:1585159 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:131552897 G>C maps to NM_001142599.1 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:131530682 C>G maps to NM_001142599.1 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr11:74000141 G>T maps to NM_182904.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr17:79803532 G>C maps to NM_000918.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:49044336 C>G maps to NM_177938.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr12:56500496 A>T maps to NM_006191.2 K72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr13:25670377 C>G maps to NM_030979.2 Y14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr13:25672057 G>T maps to NM_030979.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:40035604 G>T maps to NM_001135653.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:90690692 G>T did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:90691560 A>T did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:90690733 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:90691645 C>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr6:163510372 G>T maps to NM_152410.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:163510294 C>T maps to NM_152410.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr4:20711364 C>G maps to ENST00000503585 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr4:20715162 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr4:20706338 C>T maps to ENST00000503585 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:66006655 C>A maps to NM_018026.2 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:34499403 C>T maps to NM_020804.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr22:43280504 C>T maps to NM_001184970.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:17555288 G>T maps to NM_013358.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:17603148 C>G maps to NM_016233.2 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:17674482 C>A maps to NM_012387.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:17668534 C>T maps to NM_012387.2 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr1:17690222 C>A maps to NM_012387.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:39880796 C>A maps to NM_019088.2 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:49459325 A>T did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:55102488 G>C did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:55103863 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:55249058 G>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:103310893 G>T maps to NM_000277.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr5:43543191 A>G maps to NM_006451.4 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:43547889 C>T maps to NM_006451.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr5:138704468 G>T maps to NM_001033112.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:196547329 G>T maps to NM_002577.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:110435801 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:110439767 G>C did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:39669213 A>T maps to NM_005884.3 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:9520231 C>T maps to NM_177990.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:9546563 C>T maps to NM_177990.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr20:9523232 C>T maps to NM_177990.2 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr20:9520246 C>A maps to NM_177990.2 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr4:169835085 C>T maps to NM_001166108.1 I877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr4:169606676 C>T maps to NM_001166108.1 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr19:746309 C>T maps to NM_002579.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:734186 G>A maps to NM_002579.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:112705263 G>A maps to ENST00000413420 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:100111911 C>T maps to NM_017734.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:56720624 G>T maps to NM_001127460.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:56721406 C>T maps to NM_001127460.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:56711393 C>A maps to NM_001127460.2 *1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr12:56717635 C>T maps to NM_001127460.2 Q713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr13:28844959 C>T maps to NM_175854.7 R639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr13:28794440 C>A maps to NM_175854.7 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:91405005 C>G maps to NM_148977.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr20:3888925 G>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:167995925 C>A maps to NM_024594.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:167991021 A>G maps to NM_024594.2 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:93862490 C>T maps to NM_015368.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:93911563 G>A maps to NM_015368.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr22:50609368 C>T maps to NM_052839.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:78952808 C>G maps to NM_173797.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:39589134 G>A maps to NM_001004318.2 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr14:73719480 G>A maps to ENST00000427855 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr7:4901018 C>T maps to NM_020144.4 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:61002257 C>T maps to NM_022894.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:118989745 G>A maps to NM_002581.3 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr9:119115099 C>A maps to NM_002581.3 A1360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr9:119109372 C>G maps to NM_002581.3 V1283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:176640120 G>A maps to NM_020318.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:176709182 T>A maps to NM_020318.2 L1334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:176668392 G>A maps to NM_020318.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:176564278 C>A maps to NM_020318.2 Y513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:176564617 G>A maps to NM_020318.2 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:176640117 T>C maps to NM_020318.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:176564446 C>A maps to NM_020318.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:176709278 G>T maps to NM_020318.2 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr1:176679236 T>G maps to NM_020318.2 A1192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:176564721 C>A maps to NM_020318.2 S661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:176769216 G>A maps to NM_020318.2 R1717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:176525530 G>T maps to NM_020318.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:176564467 C>A maps to NM_020318.2 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:176738876 G>A maps to NM_020318.2 L1486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr16:3021765 G>A maps to NM_152341.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:26189844 G>A maps to NM_178422.5 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:26189346 G>A maps to NM_178422.5 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:52268163 C>T maps to ENST00000361841 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr6:52268796 C>T maps to ENST00000361841 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:142681704 G>A maps to NM_198504.2 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr3:142681704 G>C maps to NM_198504.2 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr10:34625160 C>T maps to NM_019619.3 E860E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr10:34759073 G>C maps to NM_019619.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr2:206023502 G>T maps to ENST00000406610 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr2:206480527 A>G maps to ENST00000406610 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:161990404 C>T maps to NM_004562.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr6:162683554 A>T did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr3:183585723 C>A maps to NM_018622.5 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr16:14576628 A>G maps to NM_002582.2 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:226556022 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:226555962 G>A maps to NM_001618.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:226567671 C>T maps to NM_001618.3 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:226550830 G>A maps to NM_001618.3 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr8:145058586 G>A maps to NM_032789.3 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr8:145059448 G>A maps to NM_032789.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:145059164 C>T maps to NM_032789.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr12:3931252 G>A maps to NM_020367.4 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr7:139754534 G>C maps to NM_022750.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr3:122399771 C>T maps to NM_017554.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr3:122447288 G>T maps to NM_017554.2 G1751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:122411175 C>G maps to NM_017554.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:122354847 C>G maps to NM_001113523.1 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:122354718 C>A maps to NM_001113523.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr3:122353964 C>G maps to NM_001113523.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:51980219 G>T maps to NM_001003931.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:51978870 C>T maps to NM_001003931.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr13:25049639 G>A maps to NM_006437.3 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr13:25009390 T>G maps to NM_006437.3 T1296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr13:25026686 G>C maps to NM_006437.3 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:25067871 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:50123777 C>T maps to ENST00000505697 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:122259334 G>A maps to NM_031458.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:12540005 C>T maps to NM_018222.4 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr22:44532353 G>T maps to NM_001003828.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr22:44514977 G>T maps to NM_001003828.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr22:44583691 G>T maps to NM_001137606.1 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr22:44592282 T>C maps to NM_001137606.1 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:150817143 T>A did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:150840051 C>G did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:150844594 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:150842409 G>A did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:150790038 T>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:242066100 G>A maps to ENST00000358649 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr2:242054776 C>A maps to ENST00000358649 E1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:59420424 G>C maps to NM_152716.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:59410358 C>T maps to NM_152716.2 Q681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:31724896 G>C maps to NM_014323.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr22:31722877 C>G maps to NM_014323.2 *688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr22:31741321 G>A maps to NM_014323.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr20:21689948 C>A maps to NM_006192.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr20:21687679 C>A maps to NM_006192.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr20:21687472 G>T maps to NM_006192.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:21687607 C>A maps to NM_006192.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:21687475 G>C maps to NM_006192.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr20:21695302 A>C maps to NM_006192.3 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:223085965 A>G maps to NM_181459.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr2:223085986 C>G maps to NM_181459.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr2:223163255 G>A maps to NM_181459.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr7:127251691 G>A maps to NM_006193.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr7:127253855 C>A maps to NM_006193.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:127255119 T>C maps to NM_006193.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr7:127254599 G>A maps to NM_006193.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:36923391 C>A maps to NM_016734.1 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:31815648 G>T maps to NM_001604.4 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:31812270 G>T maps to NM_001604.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:19018312 C>A maps to NM_002584.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr2:113993010 G>C maps to NM_003466.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:37132111 C>T maps to NM_006194.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:154754060 G>A maps to NM_007349.3 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:27690579 C>T maps to NM_018492.2 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr10:70051921 G>T maps to NM_022129.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:52621526 C>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:52651313 G>A maps to ENST00000296302 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr3:52623084 C>G did not map to a codon.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr1:164761953 G>C maps to NM_002585.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:32154670 G>A maps to NM_002586.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:154923708 T>C maps to NM_020524.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:66617768 G>A maps to NM_022172.2 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr11:66620275 C>A maps to NM_022172.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:66618313 C>A maps to NM_022172.2 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:66618619 G>C maps to NM_022172.2 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:136012596 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:141244803 G>A maps to NM_032420.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr5:141248634 C>T maps to NM_032420.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr4:134071447 C>G maps to NM_032961.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr4:134072194 T>C maps to NM_032961.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:134073620 C>A maps to NM_032961.1 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr4:134075493 A>T maps to NM_032961.1 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:134073526 G>A maps to NM_032961.1 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr4:134073307 C>A maps to NM_032961.1 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:134072209 G>T maps to NM_032961.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:134084204 T>C maps to NM_032961.1 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:134073055 T>A maps to NM_032961.1 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:91133297 C>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:91132790 C>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:91133514 C>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:91134038 G>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:91132997 G>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:91873531 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:91090872 A>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:91873433 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:91873654 G>C did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr23:91132572 C>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:91134107 A>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:91133245 C>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:91132778 A>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:91133649 C>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:91642835 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:91133966 G>T did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:91134265 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:91642887 C>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:91134114 A>T did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr23:91133857 G>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:91873457 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:91133467 C>G did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:91134253 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:91131778 G>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:91090589 C>A did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:91132562 G>C did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:91134170 A>G did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:91873391 C>G did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:91873447 C>T did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:91873391 C>T did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:91873711 C>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:91133882 C>A did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:91873598 C>A did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:91132499 G>T did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:91132464 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:91090612 A>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:91090519 G>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr24:4924871 G>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr24:4967430 C>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr24:4967119 T>A did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr24:4967135 C>A did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr24:4925416 G>C did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr24:5369194 C>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr24:5605739 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:141335808 G>A maps to NM_016580.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr5:141329129 T>G maps to NM_016580.2 T999T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr5:141337101 C>A maps to NM_016580.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:55569210 A>T maps to NM_001142769.1 A1538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr10:55616990 G>A maps to NM_001142763.1 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr10:55626538 C>A maps to NM_001142763.1 G1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr10:55719601 C>T maps to NM_001142763.1 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr10:55566719 G>T maps to ENST00000373965 T1558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr10:55663005 C>A maps to NM_001142763.1 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:55600179 C>A maps to NM_001142763.1 G1300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr10:55582958 A>T maps to NM_001142763.1 S1516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr10:55698650 G>T maps to NM_001142763.1 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr10:55849790 A>T maps to NM_001142763.1 Y655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr10:55626455 T>C maps to NM_001142763.1 Q1226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:55839173 G>A maps to NM_001142763.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:56106232 A>G maps to NM_001142763.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:55568916 G>A maps to NM_001142769.1 P1636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:55944934 G>A maps to NM_001142763.1 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr10:55913038 G>A maps to NM_001142763.1 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr10:55582823 G>A maps to NM_001142763.1 P1561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:55913004 C>A maps to NM_001142763.1 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr13:58208878 G>A maps to NM_001040429.2 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr13:58208863 C>G maps to NM_001040429.2 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr13:58299155 C>T maps to NM_001040429.2 Q1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr13:58208779 C>T maps to NM_001040429.2 H700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr13:58208896 T>A maps to NM_001040429.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:99662243 G>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:99661672 G>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:99662030 T>A did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr23:99663158 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:99551817 G>T did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:99551334 C>A did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:99551289 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:99661770 C>T did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:99657566 C>A did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr13:61986902 T>C maps to NM_022843.3 E443E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr13:61986931 C>A maps to NM_022843.3 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr13:61987451 C>T maps to NM_022843.3 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr13:61985740 C>A maps to NM_022843.3 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr4:31144375 G>T maps to NM_001173523.1 E1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr4:30921914 G>C maps to NM_001173523.1 A1105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr13:53422511 G>T maps to NM_002590.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr13:67477734 A>G maps to NM_203487.2 C1013C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:67799866 C>T maps to NM_203487.2 G902G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr13:67800643 A>G maps to NM_203487.2 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr13:66879050 T>A maps to NM_203487.2 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr13:67205441 G>T maps to NM_203487.2 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr13:67799734 A>T maps to NM_203487.2 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140167248 C>A maps to NM_018900.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr5:140168013 C>G maps to NM_018900.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr5:140168154 T>C maps to NM_018900.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:140166630 A>G maps to NM_018900.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140237066 G>C maps to NM_018901.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr5:140235896 G>T maps to NM_018901.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:140235692 C>A maps to NM_018901.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:140248876 G>A maps to NM_018902.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr5:140262149 C>T maps to NM_018904.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:140262129 G>T maps to NM_018904.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr5:140175374 G>T maps to NM_018905.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:140175214 C>T maps to NM_018905.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:140176273 C>A maps to NM_018905.2 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:140176676 C>T maps to NM_018905.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140180931 G>A maps to NM_018906.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140182443 C>T maps to NM_018906.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140182608 T>A maps to NM_018906.2 Y609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:140180823 G>C maps to NM_018906.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr5:140182452 C>T maps to NM_018906.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:140180985 C>A maps to NM_018906.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140188244 C>T maps to NM_018907.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140188727 G>A maps to NM_018907.2 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr5:140188232 C>T maps to NM_018907.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:140188053 C>T maps to NM_018907.2 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:140202418 C>A maps to NM_018908.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr5:140201815 G>A maps to NM_018908.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:140203603 G>A maps to NM_018908.2 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:140203688 C>T maps to NM_018908.2 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140207720 C>T maps to NM_018909.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:140208254 G>A maps to NM_018909.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr5:140208932 G>C maps to NM_018909.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:140207705 A>T maps to NM_018909.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr5:140208976 C>A maps to NM_018909.2 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr5:140208461 C>T maps to NM_018909.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr5:140209109 T>C maps to NM_018909.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr5:140209868 G>T maps to NM_018909.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr5:140215053 C>T maps to NM_018910.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:140215251 G>T maps to NM_018910.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140221175 C>T maps to NM_018911.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr5:140221265 C>T maps to NM_018911.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:140221128 C>T maps to NM_018911.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr5:140222504 C>T maps to NM_018911.2 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr5:140221313 A>G maps to NM_018911.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140229633 C>T maps to NM_031857.1 Y518Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:140229699 G>T maps to NM_031857.1 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140346533 G>A maps to NM_018899.5 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:140346558 C>A maps to NM_018899.5 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:140573660 C>T maps to NM_018930.3 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140579776 G>T maps to NM_018931.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:140580573 G>T maps to NM_018931.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140589096 G>A maps to NM_018932.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:140590314 C>T maps to NM_018932.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:140588482 G>T maps to NM_018932.3 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:140589876 C>A maps to NM_018932.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:140588646 G>C maps to NM_018932.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:140594234 G>T maps to NM_018933.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr5:140594267 A>G maps to NM_018933.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr5:140595203 G>T maps to NM_018933.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:140595314 G>T maps to NM_018933.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr5:140594627 A>G maps to NM_018933.2 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr5:140604042 A>G maps to NM_018934.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr5:140604600 G>C maps to NM_018934.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:140604158 C>A maps to NM_018934.2 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:140604376 G>T maps to NM_018934.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr5:140625808 C>G maps to NM_018935.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr5:140564335 G>A maps to NM_020957.1 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr5:140564014 C>A maps to NM_020957.1 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:140563669 C>T maps to NM_020957.1 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:140564188 G>T maps to NM_020957.1 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:140564194 T>C maps to NM_020957.1 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr5:140564053 G>A maps to NM_020957.1 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr5:140475272 C>A maps to NM_018936.2 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:140476695 C>T maps to NM_018936.2 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr5:140475549 T>C maps to NM_018936.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:140482128 G>A maps to NM_018937.2 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr5:140481579 C>A maps to NM_018937.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr5:140502857 G>C maps to NM_018938.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr5:140502218 G>C maps to NM_018938.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr5:140516575 C>T maps to NM_015669.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr5:140515708 C>A maps to NM_015669.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:140517004 C>T maps to NM_015669.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr5:140516584 G>A maps to NM_015669.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140531130 C>T maps to NM_018939.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:140531961 G>C maps to NM_018939.2 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:140530987 G>T maps to NM_018939.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140553592 C>T maps to NM_018940.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:140554147 C>A maps to NM_018940.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:140554672 C>T maps to NM_018940.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr5:140554380 C>T maps to NM_018940.2 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr5:140554281 C>T maps to NM_018940.2 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:140554587 G>T maps to NM_018940.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:140554308 C>T maps to NM_018940.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:140558863 G>T maps to NM_019120.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr5:140559231 C>G maps to NM_019120.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:140558610 C>A maps to NM_019120.2 C332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:140558301 C>A maps to NM_019120.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:140569144 G>C maps to NM_019119.3 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:140568337 A>C maps to NM_019119.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr5:140710766 C>A maps to NM_018912.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr5:140711924 C>T maps to NM_018912.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr5:140794991 T>G maps to NM_018913.2 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr5:140793344 G>A maps to NM_018913.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:140794535 G>A maps to NM_018913.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140802419 C>T maps to NM_018914.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140802923 C>T maps to NM_018914.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr5:140801891 G>T maps to NM_018914.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr5:140802624 A>T maps to NM_018914.2 K611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:140801495 C>T maps to NM_018914.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr5:140800884 C>T maps to NM_018914.2 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr5:140802856 C>G maps to NM_018914.2 S688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr5:140801373 G>T maps to NM_018914.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:140812404 G>C maps to NM_003735.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr5:140811627 G>A maps to NM_003735.2 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:140720616 G>T maps to NM_018915.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:140720358 C>T maps to NM_018915.2 H607H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140724154 C>T maps to NM_018916.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140724880 G>A maps to NM_018916.3 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140725984 G>A maps to NM_018916.3 Q795Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:140725280 G>T maps to NM_018916.3 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr5:140725243 G>A maps to NM_018916.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:140725267 C>T maps to NM_018916.3 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr5:140725165 C>T maps to NM_018916.3 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:140725486 G>A maps to NM_018916.3 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:140735546 G>T maps to NM_018917.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:140736525 C>T maps to NM_018917.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:140735936 G>T maps to NM_018917.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr5:140735555 C>T maps to NM_018917.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr5:140734862 C>A maps to NM_018917.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140745897 G>A maps to NM_018918.2 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:140744556 G>A maps to NM_018918.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:140744388 G>T maps to NM_018918.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140754621 G>A maps to NM_018919.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140755920 C>T maps to NM_018919.2 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr5:140755476 C>T maps to NM_018919.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140762864 C>T maps to NM_018920.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:140763974 C>A maps to NM_018920.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:140772973 C>T maps to NM_032088.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:140773409 A>T maps to NM_032088.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:140772460 G>T maps to NM_032088.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr5:140784057 G>C maps to NM_018921.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140784792 C>T maps to NM_018921.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140731288 C>T maps to NM_018922.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:140731776 C>G maps to NM_018922.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr5:140730486 C>T maps to NM_018922.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:140731431 C>G maps to NM_018922.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:140731746 C>A maps to NM_018922.2 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr5:140741838 C>T maps to NM_018923.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140750794 C>T maps to NM_018924.2 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:140751742 G>A maps to NM_018924.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:140751505 C>T maps to NM_018924.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr5:140768218 C>T maps to NM_003736.2 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:140769649 C>T maps to NM_003736.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr5:140768581 T>C maps to NM_003736.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:140779538 G>T maps to NM_018925.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr5:140778504 G>T maps to NM_018925.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:140787816 G>A maps to NM_018926.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:140788510 A>T maps to NM_018926.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:140789619 C>T maps to NM_018926.2 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr5:140789169 A>T maps to NM_018926.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr5:140788882 C>A maps to NM_018926.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:140799699 G>T maps to NM_018927.2 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr5:140799072 C>T maps to NM_018927.2 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr5:140798236 G>T maps to NM_018927.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr5:140857270 C>A maps to NM_002588.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr5:140856582 A>T maps to NM_002588.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:140865570 C>T maps to NM_018928.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:140866044 C>G maps to NM_018928.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr5:140871059 G>C maps to NM_018929.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:120369311 A>G maps to NM_001029996.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:82876800 C>T maps to NM_015885.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr11:82877480 G>T maps to NM_015885.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr11:82879674 G>A maps to NM_015885.3 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:82868498 G>T maps to NM_015885.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr20:56140108 C>A maps to NM_002591.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:56137947 T>A maps to NM_002591.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:82538252 C>T maps to NM_033026.5 L4459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:82579037 G>A maps to NM_033026.5 V3622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:82579133 C>T maps to NM_033026.5 K3590K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:82784885 C>T maps to NM_033026.5 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr7:82581907 A>T maps to NM_033026.5 P2787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:82430891 C>T maps to NM_033026.5 Q4983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:82538237 C>G maps to NM_033026.5 P4464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:82784243 T>A maps to NM_033026.5 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:82453630 G>A maps to NM_033026.5 S4839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr7:82579562 C>A maps to NM_033026.5 T3447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr7:82545859 C>T maps to NM_033026.5 K3814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:82583932 T>A maps to NM_033026.5 S2112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr8:17851085 G>A maps to NM_006197.3 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:52733210 G>A maps to NM_052937.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr8:52733198 C>T maps to NM_052937.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:52773686 C>A maps to NM_052937.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr21:47832812 G>A maps to NM_006031.5 V2019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr21:47851651 A>T maps to NM_006031.5 S2758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr21:47754462 A>G maps to NM_006031.5 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:47864605 G>C did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr21:47855968 C>G maps to NM_006031.5 L2968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr21:47777036 A>T maps to NM_006031.5 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:71542925 G>C maps to NM_014982.2 T1709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr14:71514571 C>T maps to NM_014982.2 S1403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr14:71444634 C>T maps to NM_014982.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:71479700 G>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:71413809 C>A maps to NM_014982.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr14:71572104 G>A maps to NM_014982.2 Q2083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr14:71575552 A>C maps to NM_014982.2 S2178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:71500229 C>T maps to NM_014982.2 Q1215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:233270785 G>A maps to NM_014801.3 F1270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:65397057 G>T maps to NM_032223.2 L1356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:65385807 C>T maps to NM_032223.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:65403085 C>T maps to NM_032223.2 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr11:65394884 G>T maps to NM_032223.2 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:65397111 C>T maps to NM_032223.2 F1374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:65396070 G>A maps to NM_032223.2 W1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr7:100205275 G>A maps to NM_002593.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:100201831 C>A maps to NM_002593.3 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:142542384 G>C maps to NM_013363.3 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:161254153 G>A maps to NM_001102566.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:95759115 C>G maps to NM_000439.4 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:95757590 C>A maps to NM_000439.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr20:17446117 T>A maps to NM_002594.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:17417377 C>T maps to NM_002594.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:1483314 G>A maps to NM_017573.3 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:78804555 C>T maps to NM_001190482.1 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:78722195 G>A maps to NM_001190482.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr15:101933581 G>A maps to NM_002570.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:101922316 G>A maps to NM_002570.3 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:117090468 G>A maps to NM_004716.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:117097993 G>T maps to NM_004716.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:70486687 C>G maps to NM_016297.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:148747745 C>T maps to NM_024028.3 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr5:148745558 C>G maps to NM_024028.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:24625899 G>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:24580608 T>A did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:24597531 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:167413427 G>A maps to NM_145859.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:167422679 C>A maps to NM_145859.1 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:105166543 G>A maps to NM_014976.1 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:105163036 C>T maps to NM_014976.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr6:170892683 C>A maps to NM_002598.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr10:112653928 T>C maps to NM_014456.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:101188049 A>G did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr11:774113 C>T did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:771357 C>T maps to NM_182612.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:165801804 C>T maps to NM_001130690.1 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:165842144 C>A did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr6:165752790 C>T maps to NM_001130690.1 K718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr6:165749634 C>A maps to NM_001130690.1 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr6:165848853 T>A maps to NM_001130690.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr6:165792837 G>T maps to NM_001130690.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:178936576 C>T maps to NM_016953.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:178592439 G>T maps to NM_016953.3 Y663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr2:183104927 G>T maps to NM_005019.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:183066249 G>A maps to NM_005019.3 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:183066210 C>G maps to NM_005019.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:54971075 C>G maps to NM_000924.3 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr7:31864548 G>T maps to NM_001191057.1 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr7:31890252 A>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr11:72290643 G>A maps to NM_002599.3 H730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr11:72294508 G>T maps to NM_002599.3 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:72316270 C>T did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr12:20766411 C>G maps to NM_000921.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:20801635 C>T maps to NM_000921.3 N860N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:20807116 C>A maps to NM_000921.3 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:20522892 C>A maps to NM_000921.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr12:20806879 G>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr12:20769196 A>C maps to NM_000921.3 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:20801619 A>T did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:20806909 C>T maps to NM_000921.3 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr12:20787989 G>C maps to NM_000921.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:14793480 A>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:14889101 T>C maps to NM_000922.3 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:10557007 C>T maps to NM_001111307.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:10578191 C>T maps to NM_001111307.1 H852H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr19:10572295 C>T maps to NM_001111307.1 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr19:18329161 C>T maps to NM_000923.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:58270780 G>A maps to NM_001104631.1 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr5:59284454 G>A maps to ENST00000502484 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr5:58285713 T>A maps to NM_001104631.1 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:144952247 G>A maps to NM_014644.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:144886152 C>T maps to NM_014644.4 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:144880778 G>A maps to NM_014644.4 S1283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:144915518 T>A maps to NM_014644.4 K636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:144952296 G>C maps to NM_014644.4 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr1:144863396 T>C maps to NM_014644.4 K2002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:144921867 T>C maps to NM_014644.4 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:144855816 C>A maps to NM_014644.4 E2246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:144882751 G>A maps to NM_014644.4 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr4:656968 C>A maps to NM_000283.3 S638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:658690 C>T maps to NM_000283.3 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr10:95380396 T>C maps to NM_006204.3 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr10:95422927 C>T maps to NM_006204.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:66639130 G>T maps to ENST00000401827 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:136512786 G>T maps to NM_018945.3 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr6:136468510 T>C maps to NM_018945.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:76714082 A>T maps to NM_003719.3 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:76640753 C>T maps to NM_003719.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:76621450 C>A maps to NM_003719.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:44108092 G>A maps to NM_002606.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:44179161 C>T maps to NM_002606.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr7:550619 G>A maps to NM_002607.5 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr22:39631863 C>A maps to NM_002608.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr22:39629505 G>A maps to NM_002608.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr4:55140743 G>A maps to NM_006206.4 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr4:55127334 G>C maps to NM_006206.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:55161432 C>T maps to ENST00000507166 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:19368219 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:19368196 T>C did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:19371287 G>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:19373468 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:19369417 T>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:96762080 T>C maps to NM_005390.4 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr4:96761852 C>T maps to NM_005390.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr11:34988249 A>G maps to NM_003477.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:34938279 A>G maps to NM_003477.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr16:335011 G>A maps to NM_006849.2 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr7:148718158 C>A maps to NM_004911.4 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr7:148716171 G>A maps to NM_004911.4 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:10930910 C>T maps to ENST00000381611 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:20370846 G>A maps to NM_174924.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:20396045 C>T maps to NM_174924.1 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:48185763 G>T maps to NM_002611.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:24544340 G>C did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:24544368 A>G did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:24483632 C>T did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:97007014 C>T maps to NM_020992.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:131607157 C>T maps to NM_003687.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:176911112 T>G maps to NM_005451.3 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr16:2636801 C>T maps to NM_002613.3 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr16:70170100 T>A maps to NM_017990.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:39878747 G>T maps to NM_001100399.1 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr13:33223008 C>T maps to ENST00000400481 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:107780270 C>T maps to NM_020381.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:107475971 T>A maps to NM_020381.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr16:15098130 G>T maps to NM_015027.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:45173563 C>T maps to NM_003681.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr21:45161590 C>G maps to NM_003681.4 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr20:1961085 G>T maps to NM_024411.4 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:69507654 C>A did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr5:32090942 G>A maps to NM_178140.2 K2463K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr5:32088002 G>C maps to NM_178140.2 P1483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:32048765 G>A maps to NM_178140.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:32088500 C>T maps to NM_178140.2 A1649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:32090545 C>A maps to NM_178140.2 S2331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:119059485 C>A maps to ENST00000392817 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:153073816 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:153072812 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:153072195 C>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:153069295 G>T did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr23:153072219 C>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:153070265 G>T did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr10:102782142 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:119044398 G>A maps to NM_173791.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:119044593 G>A maps to NM_173791.3 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr10:119043528 A>T maps to NM_173791.3 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:145748526 C>A maps to NM_002614.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:47653061 G>A maps to NM_005764.3 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:73433322 C>T maps to NM_015009.1 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:73433634 G>A maps to NM_015009.1 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:73433610 G>A maps to NM_015009.1 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr3:73433432 C>A maps to NM_015009.1 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:41966512 C>T maps to NM_001164595.1 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr1:156882413 G>T maps to NM_001080471.1 G737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:156877497 C>T maps to NM_001080471.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr8:22785203 G>T maps to NM_144962.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:4131008 G>A maps to NM_206836.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr7:94293391 G>C maps to NM_001172437.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57328600 C>T maps to NM_006210.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr19:57328546 C>T maps to NM_006210.2 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:57325528 T>C maps to NM_006210.2 G1427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:57325204 A>T maps to NM_006210.2 P1535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:57326410 G>T maps to NM_006210.2 C1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:57327337 G>T maps to NM_006210.2 T824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr19:57325480 G>C maps to NM_006210.2 A1443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:57326944 C>A maps to NM_006210.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:57326182 C>A maps to NM_006210.2 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:57328278 C>A maps to NM_006210.2 G511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:56746495 G>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:66239870 C>A maps to NM_145065.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr19:33902626 C>A maps to NM_000285.3 G257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:33878384 G>A maps to NM_000285.3 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr17:8047093 G>A maps to NM_002616.2 C854C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:8051026 C>T maps to NM_002616.2 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:239159301 A>T maps to NM_022817.2 T1119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:239184405 G>A maps to NM_022817.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:7845623 C>G maps to ENST00000377532 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:30975747 T>A maps to NM_014303.2 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:92134130 A>G maps to NM_000466.2 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:92146607 G>C maps to NM_000466.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr7:92146841 A>C maps to NM_000466.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:61258922 C>G maps to NM_002618.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr2:61258650 G>T maps to NM_002618.3 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr1:160252818 G>A maps to NM_002857.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:7361112 C>T maps to NM_001131023.1 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr3:179529587 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:179527317 C>T maps to NM_016559.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr3:179593212 T>C maps to NM_016559.1 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:179529629 C>T maps to NM_016559.1 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:42932075 G>T maps to NM_000287.3 C980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:42937457 C>A maps to NM_000287.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:53691674 C>A maps to NM_002624.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:54971968 C>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:54986325 C>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:54975506 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:54975539 C>G did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr10:6263483 C>T maps to NM_004566.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr21:45738463 G>T maps to NM_002626.4 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:48516642 G>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:48528748 C>G maps to NM_001166686.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr12:48531535 A>G maps to NM_001166686.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr10:3162112 C>T maps to NM_002627.3 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:176827198 C>A maps to NM_001029886.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr11:61018734 C>G maps to ENST00000422676 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:44104981 C>T maps to NM_000290.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr7:44104494 G>A maps to NM_000290.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:77224607 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:133294610 C>T maps to NM_001170543.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:37842246 C>T maps to NM_033419.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:28268911 T>C maps to NM_032507.3 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:28254932 A>T maps to NM_032507.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:249211703 G>T maps to NM_170725.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:249211932 C>T maps to NM_170725.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr10:50724410 T>A maps to ENST00000515869 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr10:50724809 G>A maps to ENST00000515869 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr15:34396021 A>T maps to NM_152595.4 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:41704720 C>A maps to NM_002630.3 G346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:10460559 G>A maps to NM_002631.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:77359902 G>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:77373609 A>G did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr6:49754768 G>A maps to NM_138733.4 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr6:49754267 T>A maps to NM_138733.4 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:49754843 G>A maps to NM_138733.4 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:49754753 G>T maps to NM_138733.4 Y49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr19:17631856 G>C maps to NM_012088.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:46526125 G>A maps to NM_005091.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:64097449 G>T maps to NM_002633.2 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:74062613 C>T maps to NM_173582.3 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:74047786 T>C maps to NM_173582.3 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr11:74049610 T>C maps to NM_173582.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr11:74054398 T>C maps to NM_173582.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr9:71006544 C>T maps to NM_021965.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:100920672 T>C maps to NM_000926.4 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr11:100933388 T>C maps to NM_000926.4 Q667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:100999558 C>A maps to NM_000926.4 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:118377200 C>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:118370590 A>G did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:118370481 G>T did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr6:144086521 G>T maps to NM_001100164.1 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:58342373 G>T maps to NM_080672.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr20:58318183 G>T maps to NM_080672.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr20:58322834 C>A maps to NM_080672.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr20:58416494 C>T maps to NM_080672.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:47484216 C>G did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr12:9083500 C>G maps to ENST00000433083 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr1:33836641 C>A maps to ENST00000419414 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:169815103 C>A maps to NM_024947.3 E968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:169896647 G>T maps to NM_024947.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:22208613 A>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:22115097 C>A did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr23:22065256 C>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:22186485 G>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:22095794 A>G did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:22245714 T>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:22095758 C>T did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr6:170114899 T>G maps to NM_018288.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:170105256 A>G maps to NM_018288.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr6:170112604 T>A maps to NM_018288.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:27233932 G>T maps to NM_001033561.1 S874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:6680212 C>T maps to NM_153812.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:11022090 G>T maps to ENST00000303905 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:11078409 A>G maps to ENST00000303905 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:46918458 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:46917712 G>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:46893117 A>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:46917580 C>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:46893156 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr23:46913583 G>T did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr9:123629243 C>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:123636959 G>T maps to NM_015651.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr9:96437968 C>T maps to NM_005392.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr20:34535533 C>T maps to NM_016436.4 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:133854820 C>T maps to ENST00000395386 Q818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr8:133844621 A>G maps to ENST00000395386 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:7139891 A>G maps to NM_024297.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr6:64395297 C>T maps to NM_015153.2 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr6:64404569 C>A maps to NM_015153.2 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:64421997 C>G maps to NM_015153.2 S1505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:133512082 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:133549057 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:54012306 T>C did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:54022202 G>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:54049214 C>A did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:79707135 T>A maps to NM_017934.5 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:71822069 C>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:71830998 C>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:71932780 T>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:71825206 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:71802348 C>G did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:71872437 T>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:18915419 G>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:18963196 T>C did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:18956827 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:18919705 G>C did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr16:47622820 A>T maps to NM_000293.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr16:47622892 A>G maps to NM_000293.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr16:47695707 G>T maps to NM_000293.2 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:118498594 G>A maps to NM_015157.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:118521217 C>T maps to NM_015157.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:118498321 A>C maps to NM_015157.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:111686650 A>C maps to NM_001134438.1 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:111603109 C>G maps to NM_001134438.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:111603484 T>C maps to NM_001134438.1 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:111664200 A>G maps to NM_001134438.1 K828K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:111632245 C>T maps to NM_001134438.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr3:111603563 C>T maps to NM_001134438.1 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr18:60570352 A>G maps to NM_194449.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr18:60563035 G>T maps to NM_194449.2 G746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:71715745 C>T maps to NM_015020.2 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:41750459 G>T maps to NM_003924.3 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:608827 C>T maps to ENST00000264555 S1124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:77539630 A>G maps to ENST00000427986 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:77567024 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:75737546 C>A maps to NM_015886.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr8:75757648 C>T maps to NM_015886.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr6:36931006 C>T maps to NM_153370.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:36922626 G>T maps to NM_153370.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:43804652 C>T maps to NM_002638.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr22:21107264 C>A maps to NM_058004.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr22:21096602 G>A maps to NM_058004.2 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr22:21062352 C>T maps to NM_058004.2 Q2039Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:151278829 G>A maps to NM_002651.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr18:44470756 G>A maps to NM_004671.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:73428284 C>T maps to NM_006346.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:73428245 G>C maps to NM_006346.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr13:73357624 A>G maps to NM_006346.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:85701342 G>C maps to ENST00000393343 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:85701350 G>A maps to ENST00000393343 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr11:85707959 C>T maps to ENST00000393343 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr22:38469092 G>A maps to NM_012407.3 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:502757 C>T maps to NM_001127178.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr4:517608 G>A maps to NM_001127178.1 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr4:517399 G>T maps to NM_001127178.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr4:494381 C>A maps to NM_001127178.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr14:68059353 G>A maps to NM_004569.3 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr17:16137282 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:160001448 T>A maps to NM_145167.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr18:59807679 A>T maps to NM_176787.4 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:35095563 C>A did not map to a codon.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr16:632881 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:207110614 G>A maps to NM_002644.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:207107864 G>T maps to NM_002644.3 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:207107995 C>A maps to NM_002644.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr17:26885557 G>A maps to NM_033198.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:26883209 C>T maps to NM_033198.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr17:26881994 C>T maps to NM_033198.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr17:26890463 G>A maps to NM_033198.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:26881330 G>A maps to NM_033198.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:44050035 G>T maps to NM_015937.4 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:27121694 G>T maps to NM_017837.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr3:196674942 C>T maps to NM_025163.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:196674966 G>A maps to NM_025163.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr19:49949858 C>A maps to NM_017916.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:49950681 G>T maps to NM_017916.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:49952852 G>A maps to NM_017916.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr10:98412548 C>T maps to NM_152309.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr11:17153557 T>C maps to NM_002645.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:204394050 G>A maps to NM_002646.3 R1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:204433647 C>A maps to NM_002646.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr12:18715655 G>T maps to NM_004570.4 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:18576937 C>T maps to NM_004570.4 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr12:18691230 G>A maps to NM_004570.4 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr18:39609303 A>T maps to ENST00000398870 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr18:39595530 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:178919141 G>A maps to NM_006218.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:138433507 G>A maps to NM_006219.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr3:138382871 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:138407816 C>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:9781534 G>A maps to ENST00000361110 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:106545675 C>T maps to NM_002649.2 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr7:106509388 C>G maps to NM_002649.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr7:106515249 T>G did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr7:106513330 C>A maps to NM_002649.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr7:106508803 C>T maps to NM_002649.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr5:67593335 G>T maps to ENST00000396611 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:18277948 G>T maps to NM_005027.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:18279950 C>G maps to NM_005027.2 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:46521482 G>A maps to NM_001114172.1 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:130452689 G>C maps to NM_014602.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:8785135 G>A maps to NM_001142633.1 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr17:8793401 G>T maps to NM_001142633.1 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:8753097 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:8738700 C>T maps to NM_001010855.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:209188863 A>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr2:209136332 T>C maps to NM_015040.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:209190081 G>C maps to NM_015040.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:209168914 G>A maps to NM_015040.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:209201605 C>G maps to NM_015040.3 S1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr7:99997406 G>C did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr7:99971946 G>T maps to NM_013439.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:37138630 C>A maps to ENST00000373507 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:48775871 G>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:48775921 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:71416653 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:20970991 G>A maps to NM_032409.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:20976997 G>A maps to NM_032409.2 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr9:71503910 T>C maps to NM_003558.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr9:71538234 T>C maps to NM_003558.2 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr19:3641802 G>A maps to NM_012398.2 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:15509308 G>C did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:6374625 C>A maps to NM_031220.3 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr17:6428754 G>A maps to NM_031220.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr10:3202449 G>A maps to ENST00000380989 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr10:103990394 G>T maps to NM_005029.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:130827640 C>A maps to NM_004764.4 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr12:130841572 T>C maps to NM_004764.4 Y505Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:130827213 C>T maps to NM_004764.4 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr12:130831074 G>A maps to NM_004764.4 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr12:130847602 C>T maps to NM_004764.4 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr12:130840129 G>A maps to NM_004764.4 W441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr8:22141782 C>T maps to NM_001135721.1 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:22138667 G>A maps to NM_001135721.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr22:25145672 C>G maps to NM_001008496.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr22:25145725 T>A maps to NM_001008496.2 K384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:94300722 C>T maps to NM_152431.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:68381404 T>C did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:68383036 T>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:68382647 T>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:108714607 G>A maps to NM_014819.4 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr16:2152825 G>A maps to NM_001009944.2 F2979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr16:2142538 C>T maps to NM_001009944.2 G3737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr16:2159680 C>T maps to NM_001009944.2 L1829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:2161420 G>A maps to NM_001009944.2 D1249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr16:2167521 G>A maps to NM_001009944.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr16:2141864 G>A maps to NM_001009944.2 G3818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:47835607 C>T maps to NM_138295.3 E2778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:47873942 T>C maps to NM_138295.3 P2056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:47979870 A>G maps to NM_138295.3 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr7:47968882 G>A maps to NM_138295.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:81241184 G>A maps to NM_052892.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr16:81248674 G>T maps to NM_052892.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr16:81214830 C>A maps to NM_052892.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr16:81204637 G>C maps to NM_052892.3 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr16:81151073 C>T maps to NM_052892.3 L2224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:81194498 G>A maps to NM_052892.3 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr16:81190634 G>A maps to NM_052892.3 F1318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr16:81161381 G>T maps to NM_052892.3 I2111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:88957444 C>A maps to NM_000297.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr10:102052703 C>G did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:102054793 G>T maps to NM_016112.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr22:46652799 T>C maps to NM_006071.1 E2140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:46656602 G>A maps to NM_006071.1 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:51640630 T>G maps to NM_138694.3 G2843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:51882240 G>T maps to NM_138694.3 S1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:51771112 C>A maps to NM_138694.3 V2236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr6:51640614 C>A maps to NM_138694.3 G2849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:51524708 G>T maps to NM_138694.3 C3405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:51695668 G>A maps to NM_138694.3 L2764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:51491840 G>T maps to NM_138694.3 R3913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:51890330 G>T maps to NM_138694.3 S1426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr6:51524603 G>C maps to NM_138694.3 V3440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr6:51890461 G>T maps to NM_138694.3 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr6:51907783 A>C maps to NM_138694.3 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr6:51892633 G>T maps to NM_138694.3 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr6:51924781 G>A maps to NM_138694.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:51732719 C>A maps to NM_138694.3 R2558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr8:110520438 C>A maps to ENST00000426474 R3782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr8:110406701 C>T maps to ENST00000426474 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:110471937 C>A maps to ENST00000426474 L2373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr8:110437405 A>T maps to ENST00000426474 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr8:110453070 C>T maps to ENST00000426474 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:110523030 T>A maps to ENST00000426474 A3808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:110463360 C>T maps to ENST00000426474 V2111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:110439381 A>T maps to ENST00000426474 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:110535547 T>C maps to ENST00000426474 S4140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr8:110457074 A>G maps to ENST00000426474 P1659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:110476644 A>T maps to ENST00000426474 I2528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:110509431 C>A maps to ENST00000426474 A3510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:155263134 C>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:155265281 C>A maps to ENST00000423816 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:155264484 G>A maps to ENST00000423816 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:155264346 G>T maps to ENST00000423816 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:14574958 G>T maps to NM_213560.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:14552022 G>T maps to NM_213560.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr19:14574646 G>A maps to NM_213560.1 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:89279242 G>T maps to NM_006256.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr9:131479169 C>A maps to NM_013355.3 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr11:125267789 C>A maps to NM_022062.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:32996236 G>T maps to NM_004572.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:33021917 A>G maps to NM_004572.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:399029 C>T maps to NM_007183.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:159499162 C>T maps to NM_003628.3 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:159481409 C>A maps to NM_003628.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr2:159481742 G>C maps to NM_003628.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:159536993 A>G maps to NM_003628.3 A1128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:159536981 G>A maps to NM_003628.3 K1124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr3:119348281 T>A maps to NM_015900.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr4:110635634 C>A maps to NM_030821.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:20501519 G>T maps to NM_001105572.1 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:20249203 C>A maps to NM_014589.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr22:31533954 G>T maps to NM_015715.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:186880433 C>T maps to NM_024420.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:186934539 G>T did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:186946789 T>C maps to NM_024420.2 Y610Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-18-3409-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:48603038 C>T maps to NM_003706.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:42379557 G>A maps to NM_178034.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr15:42378497 C>T maps to NM_178034.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr15:42379859 G>T maps to NM_178034.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:42279559 G>A maps to NM_001080490.1 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:42442309 C>A maps to ENST00000397272 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr15:42445843 C>T maps to ENST00000397272 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr1:20412683 G>A maps to NM_000929.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:46672347 G>T maps to NM_001168357.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:160806153 G>C maps to NM_007366.4 S1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:59811057 C>A maps to NM_173801.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:57079511 C>A maps to NM_002655.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr8:57078945 A>T maps to NM_002655.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:57079299 C>T maps to NM_002655.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr20:30784524 G>A maps to NM_002657.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:44169568 G>C maps to NM_002659.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:44159725 C>T did not map to a codon.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr2:28802549 C>T maps to NM_153021.4 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr12:14659941 G>T maps to NM_024829.5 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:113812700 C>T maps to NM_173542.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr20:8707971 T>C maps to NM_015192.2 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr20:8609071 G>T maps to NM_015192.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr20:8713909 G>A maps to NM_015192.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr20:8862384 T>C maps to NM_015192.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:64026123 G>T maps to NM_000932.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr11:64032798 C>T maps to NM_000932.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:64022420 G>T maps to NM_000932.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr20:9317804 C>T maps to NM_001172646.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr20:9434025 G>A maps to NM_001172646.1 T971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr20:9404576 A>G maps to NM_001172646.1 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr20:9388676 A>T maps to NM_001172646.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:9401950 C>G maps to NM_001172646.1 S721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr20:9371210 C>A maps to NM_001172646.1 C424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:38052852 G>A maps to NM_001130964.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr17:43195802 C>A maps to NM_133373.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr2:219501077 T>A maps to ENST00000432688 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:219499247 C>A maps to ENST00000432688 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:96006326 C>T maps to ENST00000371380 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr10:96039544 C>T maps to ENST00000371380 Q1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:96033437 A>G maps to ENST00000371380 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr10:95790938 C>A maps to ENST00000371380 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:96018840 G>T maps to ENST00000371380 E1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr20:39802169 T>C maps to NM_002660.2 F1130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr20:39802789 C>T maps to NM_002660.2 F1224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr16:81819731 C>T maps to NM_002661.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr16:81965178 G>T maps to NM_002661.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:155200016 A>G maps to ENST00000340059 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr3:155211981 G>A maps to ENST00000340059 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:155206554 T>A maps to ENST00000340059 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:155203418 T>G maps to ENST00000340059 V908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:155203418 T>C maps to ENST00000340059 V908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:155203197 G>T maps to ENST00000340059 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr3:155203220 G>A maps to ENST00000340059 D974D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr3:155232541 C>A maps to ENST00000340059 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:2415981 C>A maps to NM_014638.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:198948735 G>A maps to NM_006226.3 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr2:198950159 C>G maps to NM_006226.3 S640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:198948852 T>G maps to NM_006226.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:198949014 T>C maps to NM_006226.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr2:198950526 G>A maps to NM_006226.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:198950308 G>T maps to NM_006226.3 G690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:198949213 A>T maps to NM_006226.3 K325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:17051497 C>T maps to NM_001144382.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:215977 C>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:205452 G>T did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr5:41382016 C>T maps to NM_001005473.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr5:41382439 G>T maps to NM_001005473.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr5:41382436 G>A maps to NM_001005473.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:41382262 G>C maps to NM_001005473.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:18854646 T>A maps to ENST00000266505 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr12:18841146 G>A maps to ENST00000266505 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:171405269 C>T maps to NM_002662.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr3:171320966 T>C maps to NM_002662.3 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:171406666 C>G did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:171427429 G>A maps to NM_002662.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr17:4720514 C>T maps to NM_002663.3 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:40876044 G>A maps to NM_012268.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:105398140 G>A maps to NM_138790.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:242253242 C>T maps to NM_152666.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr1:242287913 T>C maps to NM_152666.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:144998323 C>A maps to NM_201380.2 E2062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr8:144997745 C>A maps to NM_201380.2 L2254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:144996740 G>A maps to NM_201380.2 I2589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:145049348 G>A maps to NM_000445.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr8:144993461 G>A maps to NM_201380.2 T3646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:145006372 C>T maps to NM_201380.2 E806E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr8:145006635 C>A maps to NM_201380.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:144993254 G>T maps to NM_201380.2 G3715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr8:144991187 C>A maps to NM_201380.2 L4404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:144992858 G>C maps to NM_201380.2 L3847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:144998186 C>T maps to NM_201380.2 A2107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr8:144993707 C>G maps to NM_201380.2 L3564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr8:144993527 C>A maps to NM_201380.2 V3624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:68607525 A>T maps to NM_002664.2 K37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:68608006 C>G maps to NM_002664.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr10:124175427 G>T maps to NM_021622.4 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr10:124177425 G>A maps to NM_021622.4 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr8:38808483 G>T maps to NM_021623.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:19413941 C>A maps to ENST00000429027 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:19473548 A>G maps to ENST00000429027 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:204228609 C>A maps to ENST00000367191 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:204210870 G>T maps to ENST00000367191 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:204197298 T>G maps to ENST00000367191 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:16863214 G>A maps to ENST00000448080 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr7:30101577 C>T maps to ENST00000440706 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:45567134 C>A maps to ENST00000256692 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr12:45568067 G>T maps to ENST00000256692 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:131897810 G>T maps to ENST00000409158 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:30164859 C>T maps to ENST00000436066 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:151121853 G>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:151121911 G>A maps to NM_001029884.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:151107544 G>T maps to NM_001029884.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:151121995 C>G maps to NM_001029884.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:151161514 C>G maps to NM_001029884.1 S1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:39914664 C>T maps to NM_022835.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr19:39912891 G>T maps to NM_022835.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr19:39914207 A>G maps to NM_022835.2 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:65207902 C>T maps to ENST00000394691 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr14:65203601 C>T maps to ENST00000394691 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr14:65197884 C>T maps to ENST00000394691 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr14:65209877 C>G maps to ENST00000394691 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr16:67316120 A>T maps to NM_001129729.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:67316210 G>A maps to NM_001129729.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:67322175 G>T maps to NM_001129729.1 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr16:67318230 G>T maps to NM_001129729.1 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr16:67314218 C>G maps to NM_001129729.1 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:143300 C>T maps to NM_052909.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:161980 G>C maps to NM_052909.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr5:163558 G>T maps to NM_052909.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:93147975 G>A maps to NM_001004330.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:93147928 C>T maps to NM_001004330.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr2:43986037 G>A did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr2:43926840 C>T maps to NM_172069.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr2:43927290 A>T maps to NM_172069.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:40826031 C>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr17:43515289 C>A maps to NM_014798.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:43552913 C>A maps to NM_014798.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:16054793 C>A maps to ENST00000420314 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:16053733 C>T maps to ENST00000420314 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:208841612 G>A maps to NM_001080475.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:208725976 C>A maps to NM_001080475.2 G654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr15:65153738 C>T maps to NM_025201.4 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr6:161139407 C>T maps to NM_000301.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:161132157 G>T maps to NM_000301.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:90210934 G>A maps to NM_002666.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr9:19120959 G>T maps to NM_001122.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:4512462 G>T maps to NM_001080400.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:23700939 C>T maps to NM_005030.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr16:23695280 G>T maps to NM_005030.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr20:21142510 G>C did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:21143632 G>A maps to NM_018474.4 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr5:57752857 G>C maps to NM_006622.2 S357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr1:45267394 C>T maps to NM_004073.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:128812735 C>T maps to NM_014264.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr4:128819592 G>C did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:118880182 C>T maps to NM_002667.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:12024742 C>T maps to ENST00000376369 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:12017936 C>T maps to ENST00000376369 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr7:100855936 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:100855819 C>G maps to NM_001084.4 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:103041627 G>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:103043404 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:103042766 T>C did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:49029809 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:49029581 T>G did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr4:155461790 C>A maps to NM_002669.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr4:155467272 A>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:142408473 G>A maps to NM_001172312.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr3:142408473 G>C maps to NM_001172312.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:114880809 G>A did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:114871182 G>C did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:114871193 G>A did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr20:44538309 G>A maps to NM_006227.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:17476592 G>A maps to NM_031310.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr19:17476989 G>A maps to NM_031310.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr19:17476368 G>C maps to NM_031310.1 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr19:17477001 G>A maps to NM_031310.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:37228712 T>G maps to NM_020405.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:126736308 C>T maps to NM_032242.3 A1106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:126751654 C>T maps to NM_032242.3 S1857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:126747834 G>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:126724012 C>T maps to NM_032242.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr3:126732959 G>T did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:126708342 G>T maps to NM_032242.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:208212980 G>A maps to NM_025179.3 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:208390373 G>A maps to NM_025179.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:208219237 C>T maps to NM_025179.3 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:208390970 G>T maps to NM_025179.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:153698897 G>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:153692516 C>G did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:153695767 C>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:153688714 G>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:153692006 C>G did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:153689014 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:132193131 G>A maps to NM_020911.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr7:131883283 C>A maps to NM_020911.1 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:131870089 G>A maps to NM_020911.1 I1042I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:131895860 G>C maps to NM_020911.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr7:131870116 G>C maps to NM_020911.1 V1033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:131865380 G>T maps to NM_020911.1 C1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr7:132193311 G>C maps to NM_020911.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr7:131887565 C>A maps to NM_020911.1 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:131817906 G>A maps to NM_020911.1 N1830N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr22:50724255 G>A maps to NM_012401.2 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr22:50714335 C>T maps to NM_012401.2 T1798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr22:50720444 A>C maps to NM_012401.2 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr22:50719565 C>A maps to NM_012401.2 E1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:50718175 G>A maps to NM_012401.2 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr23:153036445 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:153040420 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:153043731 A>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:153043054 G>T did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr12:94618034 C>T maps to NM_005761.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr12:94603389 A>G maps to NM_005761.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr12:94543740 A>T maps to NM_005761.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:94697542 T>A maps to NM_005761.1 T1466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:94575246 C>G maps to NM_005761.1 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:129278575 G>A maps to NM_015103.2 I1728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr3:129290354 G>A maps to NM_015103.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr3:129284821 A>T maps to NM_015103.2 I1410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:129282077 C>T maps to NM_015103.2 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:129286442 G>A maps to NM_015103.2 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:129290378 G>A maps to NM_015103.2 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr3:129290098 C>T maps to NM_015103.2 G1128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:205801750 G>A maps to NM_152491.4 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:205817011 C>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr20:56227336 C>T maps to NM_020182.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr20:56227420 G>A maps to NM_020182.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:72188301 G>A maps to NM_031293.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr16:72159292 C>G maps to NM_031293.2 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:72153939 C>G maps to NM_031293.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:74326831 G>T maps to NM_033238.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr22:41980048 C>A maps to NM_002676.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:82359588 A>T maps to NM_002677.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr9:139311656 G>A maps to NM_015160.1 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr9:139311536 G>A maps to NM_015160.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:190719767 C>A maps to NM_000534.4 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr7:6026708 G>A maps to NM_000535.5 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:6045586 C>T maps to NM_000535.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr7:6038906 C>A did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:152937079 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:152937125 G>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:152936759 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:152936584 C>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:152937049 C>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr2:219204776 C>A maps to NM_015488.4 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr10:118321052 G>A maps to NM_000936.2 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr10:118314757 A>T maps to NM_000936.2 K214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr10:118364921 C>G maps to NM_006229.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr10:118363605 T>A maps to NM_006229.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr10:118385515 G>A maps to NM_005396.4 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr10:118389529 G>T maps to NM_005396.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr10:118401631 C>A maps to NM_005396.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr10:118196341 C>T maps to NM_001011709.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:118220598 T>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:152226043 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:152225748 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:152159310 G>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:152159170 G>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:152158902 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:152159450 A>C did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr23:152159318 T>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:46973038 A>C maps to NM_018215.3 S418S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-66-2754-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr19:46998323 C>T maps to ENST00000377652 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:46998641 C>A maps to NM_020709.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr17:37825906 C>T maps to NM_002686.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:39650826 G>T maps to NM_002687.3 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:68385525 A>G maps to NM_020143.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr11:822470 C>T maps to NM_020376.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr11:822506 C>A maps to NM_020376.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr22:44323025 G>T maps to NM_025225.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:7880068 C>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:7894052 G>A did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr22:44280220 C>G maps to ENST00000216177 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr22:44285397 C>A maps to ENST00000216177 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr19:7606544 C>T maps to NM_001166111.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:7620513 A>G maps to NM_001166111.1 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:7605532 G>T maps to NM_001166111.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr7:108119673 C>T maps to NM_015723.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr2:55895076 G>C maps to NM_033109.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:55870349 T>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:55899141 G>A maps to NM_033109.3 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:89818972 C>A maps to NM_172240.2 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:53544159 G>A maps to NM_153703.4 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:53547778 G>A maps to NM_153703.4 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:53535730 C>T maps to NM_153703.4 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:127387382 C>T maps to NM_015720.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:84560849 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:84563146 G>A did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr21:46702292 C>G maps to NM_133635.4 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:166818625 C>G maps to NM_017542.3 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:24741282 C>T did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:24760117 G>C did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:24751920 C>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:24721416 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:24859850 C>T did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:24733278 G>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:24766500 G>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:24753604 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:24741270 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:65062096 C>T maps to NM_002689.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr11:65062069 C>T maps to NM_002689.2 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:42196566 C>T maps to NM_002690.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr19:50918709 G>T maps to ENST00000391817 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:133218805 G>A maps to ENST00000455752 D1713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:133256809 T>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr12:133201571 C>G maps to ENST00000455752 L2225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr12:133215751 C>A maps to ENST00000455752 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr14:50130031 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:89872199 G>A maps to NM_002693.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr5:74892911 G>T maps to NM_016218.2 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr3:121151796 G>A maps to ENST00000393672 L2680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:121206413 C>A maps to ENST00000393672 G1924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:121208372 C>T maps to ENST00000393672 E1271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:86258524 G>A maps to NM_015425.3 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:86297335 G>A maps to NM_015425.3 H557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:86267660 C>G maps to NM_015425.3 L1198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:86292413 G>A maps to NM_015425.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:113308537 C>T maps to NM_019014.4 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr17:7415643 C>T maps to NM_000937.4 P1491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr4:57889494 G>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr4:57897087 C>G maps to NM_000938.1 Y1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:128610592 C>A maps to NM_004805.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:1094002 A>C maps to NM_002695.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:79745902 G>A maps to NM_007055.3 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:79777380 C>A maps to NM_007055.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr12:106890609 C>T maps to NM_018082.5 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:106903245 G>A maps to NM_018082.5 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:106824223 G>A maps to NM_018082.5 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr12:106889911 A>C maps to NM_018082.5 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr8:22107638 C>T maps to NM_001722.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:145460114 C>T maps to NM_032305.1 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr22:41926858 G>A maps to NM_138338.3 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:621339 C>G maps to NM_005035.3 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr7:72413684 C>G maps to ENST00000434423 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:72409130 C>G maps to ENST00000434423 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr7:75051284 G>T maps to ENST00000257665 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr7:75051113 G>A maps to ENST00000257665 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr7:53103840 C>T maps to NM_182595.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr7:53103630 G>A maps to NM_182595.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:53103777 C>A maps to NM_182595.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr7:53103759 G>C maps to NM_182595.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr7:53104038 G>T maps to NM_182595.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr7:53104164 C>T maps to NM_182595.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:53103588 C>T maps to NM_182595.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr1:46660017 G>T maps to ENST00000371986 C269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr9:134394306 C>T maps to NM_007171.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr9:134393911 C>T maps to NM_007171.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr14:77746414 G>A maps to NM_013382.5 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:94937441 G>A maps to NM_000446.5 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:94947700 G>A maps to NM_000446.5 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:99149121 G>C maps to NM_015029.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:99149136 C>A maps to NM_015029.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr3:119367436 G>A maps to NM_022135.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr6:105609427 C>T maps to NM_022361.4 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:105609376 A>T maps to NM_022361.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr23:48378760 A>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:48372702 G>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:48369715 T>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr13:38143435 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:124499072 G>A maps to NM_015450.2 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr8:43155764 A>T maps to NM_001005365.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr8:43155725 C>A maps to NM_001005365.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr8:43197381 C>G maps to NM_001005365.2 S424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:132021446 G>T maps to NM_001083538.1 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:132021607 C>A maps to NM_001083538.1 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:131976355 C>A maps to NM_001083538.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr2:131976175 C>T maps to NM_001083538.1 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:131976313 C>T maps to NM_001083538.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr2:132010528 C>T maps to NM_001083538.1 H545H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr14:19553634 G>A maps to NM_001005356.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:19553803 G>T maps to NM_001005356.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr3:87311290 G>A maps to NM_001122757.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:167382319 A>G maps to NM_002697.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:167370722 A>G maps to NM_002697.3 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:42600275 G>T maps to ENST00000342301 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:120176495 T>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:120178197 G>A maps to NM_014352.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:99283999 G>T maps to NM_005604.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:105473020 C>A maps to NM_006236.1 Y351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr2:105473368 C>A maps to NM_006236.1 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:82763670 C>T did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:82763522 G>C did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:82763714 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr13:79175663 G>T maps to NM_006237.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr13:79175768 A>G maps to NM_006237.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr4:147561308 G>T maps to NM_004575.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr7:39125631 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr10:71974267 T>C maps to NM_021129.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr10:71969328 T>A maps to NM_021129.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr5:54721825 G>C maps to NM_176895.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr1:56989494 C>G maps to NM_003713.4 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:122348812 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:134165635 C>T maps to NM_032728.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:134183308 G>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr22:46611133 C>T maps to NM_001001928.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:35392323 C>G maps to NM_006238.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr6:35393714 C>G maps to NM_006238.4 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr4:23803869 G>A maps to NM_013261.3 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr4:23816006 C>A maps to NM_013261.3 G367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr5:149212300 C>A maps to NM_133263.3 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr5:149216147 G>A maps to NM_133263.3 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr5:149213088 G>T maps to NM_133263.3 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr4:57269555 A>G maps to NM_002703.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:18767942 A>G did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:18845391 A>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:18775753 G>A did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:18797253 T>A did not map to a codon.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr23:18725906 G>A did not map to a codon.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr4:76788551 G>T maps to NM_006239.2 S557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:76805904 G>A maps to NM_006239.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:76811181 C>A maps to NM_006239.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:70224134 G>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:70171653 G>T maps to NM_003626.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:70118485 G>T maps to NM_003626.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:81741341 C>T maps to NM_003625.2 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:81839427 C>G maps to NM_003625.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:81839365 A>T maps to NM_003625.2 L180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr12:81839427 C>A maps to NM_003625.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:81675036 G>A maps to NM_003625.2 R1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:81688781 T>A maps to NM_003625.2 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr19:49636537 C>T maps to NM_003660.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr19:49631294 A>G maps to NM_003660.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:203037725 G>T maps to ENST00000367238 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:203036821 G>C did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr12:27832533 C>A maps to NM_003622.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:27829479 G>T maps to NM_003622.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr12:27820097 G>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:7672957 C>T maps to NM_003621.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr11:7670764 C>T maps to NM_003621.2 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr12:42729761 C>A maps to NM_016488.6 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:143767486 C>T maps to NM_001123068.1 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:143767818 G>A maps to NM_001123068.1 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:170465178 A>G did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:170493660 A>T maps to NM_004792.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr22:22039087 A>T maps to NM_148175.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr6:149854711 T>A did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr5:102472514 C>G maps to ENST00000451606 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr16:4934185 C>A maps to NM_002705.4 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr16:4934562 G>T maps to NM_002705.4 R1365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:57033099 G>A maps to NM_014906.3 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr17:56833426 C>A maps to NM_014906.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:57057443 C>A maps to NM_014906.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr4:89199699 A>G maps to NM_152542.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:160474329 C>G maps to NM_139245.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:30577616 G>A maps to NM_002714.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:30572488 C>A maps to NM_002714.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr12:80203634 T>A maps to NM_001143885.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:202400695 G>T maps to ENST00000367270 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:104206337 G>A maps to NM_015316.2 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:104206295 G>A maps to NM_015316.2 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:104208263 G>C maps to NM_015316.2 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr14:104206649 C>A maps to NM_015316.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr14:104202519 A>G maps to NM_015316.2 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr14:104251218 C>A maps to NM_015316.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr19:45899465 C>T maps to NM_001142502.1 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:45885826 C>A maps to NM_001142502.1 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:45885787 G>A maps to NM_001142502.1 F815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:45888901 G>A maps to NM_001142502.1 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:64013995 C>T maps to NM_138689.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr19:49377886 C>G maps to NM_014330.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:204379711 C>A maps to NM_032833.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:204380188 G>A maps to NM_032833.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:204380248 T>C maps to NM_032833.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr20:37531332 C>T maps to NM_015568.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:113558612 G>A maps to NM_002711.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr7:113519604 A>G maps to NM_002711.3 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr7:113518036 G>T maps to NM_002711.3 S1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr7:113517798 T>C maps to NM_002711.3 K1116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr8:8998699 G>T maps to NM_024607.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr8:8998582 G>T maps to NM_024607.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:93389947 C>T maps to NM_005398.4 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:49143530 C>G did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:49143512 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:49142923 A>C did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr7:94827676 G>T maps to NM_001166160.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr7:94540120 G>T maps to NM_001166160.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:94540110 C>G maps to NM_001166160.1 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr17:48226575 G>A maps to NM_032595.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr17:48212998 C>T maps to NM_032595.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:48216852 C>A maps to NM_032595.3 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:133534874 G>A maps to NM_002715.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:52724337 C>T maps to NM_014225.5 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr19:52705204 C>T maps to NM_014225.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:111618705 A>G maps to NM_181699.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:133769241 G>T maps to ENST00000455566 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr3:135768130 T>A maps to NM_002718.4 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:322172 C>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr11:64694349 C>T maps to NM_006244.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr11:64695362 G>A maps to NM_006244.3 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr14:63851286 C>A maps to ENST00000422769 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr4:101953521 C>A did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:22368618 C>T maps to ENST00000397775 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:22386062 G>T maps to ENST00000397775 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:68415795 C>A maps to ENST00000406334 G14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:104356756 G>T maps to NM_147180.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr9:104356828 C>G maps to NM_147180.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:104356945 G>A maps to NM_147180.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr18:9570623 T>C maps to NM_001042388.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr18:9557343 C>A maps to NM_001042388.1 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:73108203 C>T maps to NM_174907.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr14:94712741 C>A maps to NM_058237.1 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:94731757 C>G maps to NM_058237.1 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:46878997 C>T maps to NM_006247.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:127912173 G>A maps to NM_001123355.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr10:103908179 G>T maps to NM_015062.3 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr10:103898670 A>G maps to NM_015062.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:47087787 C>T maps to NM_005972.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr10:47086885 C>T maps to NM_005972.4 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:48931478 G>C did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:8563165 C>A maps to NM_032152.4 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:8564040 C>T maps to NM_032152.4 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:22890617 G>A maps to NM_206954.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:22893283 C>T maps to NM_206954.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:12854132 C>A maps to NM_023013.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:12854103 G>T maps to NM_023013.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:12835766 C>A maps to NM_001080830.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr1:13448271 G>A maps to NM_001024661.1 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr1:12921408 C>T maps to NM_023014.1 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:12919946 G>A maps to NM_023014.1 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:12921336 C>T maps to NM_023014.1 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:12920018 A>T maps to NM_023014.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:12979851 C>A maps to NM_001012277.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr12:11507477 C>T maps to NM_005039.3 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:11546402 T>G maps to NM_006248.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:11461805 T>C maps to NM_002723.3 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr15:91528041 C>A maps to NM_003981.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:91524152 G>T maps to NM_003981.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr15:91513657 A>T maps to NM_003981.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:106555117 G>T maps to NM_001198.3 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:129784609 G>A maps to NM_020228.2 Q948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:129800973 C>T maps to NM_020228.2 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:45246119 G>A maps to NM_020229.2 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr9:133556879 C>T maps to NM_021619.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr9:133542180 G>A maps to NM_021619.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:100061956 C>G maps to ENST00000359773 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:100062258 C>A maps to ENST00000359773 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr8:70981879 C>A maps to NM_024504.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr8:70980717 T>C maps to NM_024504.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:70981440 G>A maps to NM_024504.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:3322186 C>A maps to NM_022114.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:3102983 C>T maps to NM_022114.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:14108528 G>A maps to NM_012231.4 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr1:14105510 A>C maps to NM_012231.4 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr12:108145614 G>A maps to NM_012406.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr4:121738063 T>A maps to NM_018699.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr4:121616415 A>T maps to NM_018699.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:121774679 C>A maps to NM_018699.2 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:81124466 C>T maps to NM_001099403.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr5:23510027 G>C did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr5:23510042 C>T maps to NM_020227.2 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:23526522 A>T maps to NM_020227.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr5:23510029 T>C maps to NM_020227.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:23527569 C>A maps to NM_020227.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr5:23527440 T>C maps to NM_020227.2 Y748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr5:23527404 C>A maps to NM_020227.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr5:23523401 C>A maps to NM_020227.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:23521147 C>A maps to NM_020227.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr5:23526955 C>A maps to NM_020227.2 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:45980645 T>C maps to NM_181697.1 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:23689671 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:23685869 G>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr1:173455422 G>C maps to NM_004905.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:27355471 T>G maps to NM_013388.4 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr5:145199570 T>C maps to NM_182960.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:203452365 C>T maps to NM_201348.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:203455861 C>T maps to NM_201348.1 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr6:105821373 G>A maps to NM_002726.4 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr20:47249124 G>A maps to NM_020820.3 I1440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:47292763 G>A maps to NM_020820.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr20:47248918 G>A maps to NM_020820.3 N1474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:47444244 G>A maps to NM_020820.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr20:47259001 C>T maps to NM_020820.3 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr20:47307608 G>A maps to NM_020820.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:69104661 T>A maps to NM_024870.2 A1502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:69030877 A>T maps to NM_024870.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr8:69000006 G>A maps to NM_024870.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:68984804 G>A maps to NM_024870.2 Q523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr8:69050753 T>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr8:68931876 C>T maps to NM_024870.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:72358636 C>T maps to NM_005041.4 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:72358510 G>T maps to NM_005041.4 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr10:72360181 G>T maps to NM_005041.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr11:57148123 G>A maps to NM_006093.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:186277346 G>A maps to NM_005807.3 K832K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:186276764 G>A maps to NM_005807.3 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:186277376 T>A maps to NM_005807.3 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:186277487 G>A maps to NM_005807.3 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr12:11082903 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr13:28562753 G>A maps to NM_001105577.1 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:62198493 G>A maps to NM_001037335.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr20:62195013 G>A maps to NM_001037335.2 Q1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr20:62196784 G>A maps to NM_001037335.2 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:42864062 T>G maps to NM_153026.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:64085477 G>T maps to NM_198859.3 S595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:64184591 C>A maps to NM_198859.3 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:64133034 G>A maps to NM_198859.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:64142966 C>A maps to NM_198859.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr3:64133178 G>T maps to NM_198859.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:49032244 G>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:49032070 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:49034342 G>A did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr6:41754617 G>T maps to NM_013397.5 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:57144980 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:57512647 C>T maps to NM_000947.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:57398139 C>A maps to NM_000947.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:57472356 A>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:57512470 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr6:57512690 G>T maps to NM_000947.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:57472428 A>G maps to NM_000947.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:57157065 G>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:151292540 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:219692565 C>T maps to NM_017431.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:66519040 G>T maps to NM_212472.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr7:720267 C>A maps to NM_002735.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:106781374 T>G maps to NM_002736.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:106786782 T>C maps to NM_002736.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr7:106710739 C>T maps to NM_002736.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr16:24135244 G>A maps to NM_002738.6 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr11:6340730 G>A maps to NM_145040.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:54401226 C>A maps to NM_002739.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:54401274 C>A maps to NM_002739.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr19:54410100 C>T maps to NM_002739.3 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr3:170002299 G>A maps to NM_002740.5 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr3:170016899 T>G did not map to a codon.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr19:11559429 G>A maps to ENST00000436195 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:11559426 C>T maps to ENST00000436195 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:11547297 C>T maps to ENST00000436195 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:2105396 C>T maps to NM_002744.4 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:2077515 C>T maps to NM_002744.4 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr14:30105515 C>T maps to NM_002742.2 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr14:30066793 G>A maps to NM_002742.2 G779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr14:30066892 G>A maps to NM_002742.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr19:47219576 C>A maps to ENST00000449438 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:47197342 G>A maps to ENST00000449438 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr19:47200992 C>G maps to ENST00000449438 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:47207525 C>A maps to ENST00000449438 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:37543625 T>C maps to NM_005813.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr8:48711772 G>C maps to NM_006904.6 S3431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:48719887 C>T did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:48869796 T>C maps to NM_006904.6 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr8:48743255 G>C maps to NM_006904.6 V2768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr10:53564376 C>A maps to NM_001098512.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr10:54048747 G>A maps to NM_001098512.1 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr4:82096030 C>A maps to NM_006259.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:179315082 C>A maps to NM_003690.4 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:76076957 G>A maps to NM_004705.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:3544546 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:3573383 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:22287672 G>C maps to ENST00000397199 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr5:35065616 G>A maps to NM_000949.4 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr5:35065412 C>A maps to NM_000949.4 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:35086374 G>T maps to NM_000949.4 C46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr5:35065606 C>A maps to NM_000949.4 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr5:35065577 C>A maps to NM_000949.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:50185234 C>T maps to NM_001536.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr21:48068368 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:23393851 G>A maps to NM_006109.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:3649957 G>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:4705265 G>T maps to NM_012409.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:4680513 C>A maps to NM_001080123.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:36302947 C>T maps to NM_021232.1 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:68882194 G>T maps to NM_138964.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:5283321 C>A maps to NM_144773.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr20:5294817 G>A maps to NM_144773.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:5283024 C>T maps to NM_144773.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:71275311 A>T maps to NM_021225.4 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:15995678 A>G maps to NM_006017.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr4:16034999 G>A maps to NM_006017.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:95944748 G>T maps to NM_144707.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:177421250 C>T maps to NM_006261.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:177419910 T>A maps to NM_006261.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr5:177422883 G>T maps to NM_006261.4 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr5:177422871 C>T maps to NM_006261.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:93603659 T>C maps to NM_000313.3 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:214178590 G>A maps to NM_002763.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr1:214170586 C>T maps to NM_002763.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:214171383 C>T maps to NM_002763.3 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:75321912 C>T maps to ENST00000445876 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr14:75321888 C>T maps to ENST00000445876 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:60665635 G>C maps to NM_014502.4 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:60671207 C>A maps to NM_014502.4 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:52870480 G>T maps to NM_032864.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:153528971 C>G did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr2:153519148 G>A maps to ENST00000410080 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:153532917 C>G did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:50028963 C>A maps to NM_001031698.1 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr20:62660758 G>T maps to NM_012469.3 E821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:1582316 G>A maps to NM_006445.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr12:49691237 G>T maps to ENST00000451891 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr12:49689165 T>C maps to ENST00000451891 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:106885650 G>T did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:106888415 C>T did not map to a codon.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr7:18067279 C>A maps to NM_175886.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:12817406 G>T did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:12827450 G>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr19:50099157 G>A maps to NM_020719.1 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:50097966 A>T maps to NM_020719.1 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:120021725 G>T maps to NM_016644.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr5:120021650 G>A maps to NM_016644.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr5:120022384 C>A maps to NM_016644.1 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr5:120021830 C>G maps to NM_016644.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:240982213 C>T maps to NM_001080835.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:240982174 G>T maps to NM_001080835.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:138739122 G>A maps to NM_001013650.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:138739281 G>A maps to NM_001013650.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:36467878 C>T maps to NM_001160167.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:36472838 C>A maps to NM_001160167.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr11:36484108 G>T maps to NM_001160167.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:37312653 C>G did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr23:37312767 G>C did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:150869318 G>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:150868562 G>C did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:150869313 G>C did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:29824891 G>T maps to NM_145239.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:9991145 G>A maps to NM_207351.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:132484621 G>T maps to NM_016307.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:142460324 G>A maps to ENST00000486171 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr4:119203395 G>A maps to NM_003619.3 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:119203130 G>C maps to NM_003619.3 S863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr4:119220047 T>C maps to NM_003619.3 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr16:2868806 C>T maps to NM_006799.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr6:84233820 G>T maps to NM_153362.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:84234167 C>A maps to NM_153362.2 Y336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:84233921 C>G maps to NM_153362.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr6:84234197 C>T maps to NM_153362.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr7:141536909 A>T did not map to a codon.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr3:46785593 C>T maps to ENST00000331814 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:31098056 G>C maps to NM_001039503.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr8:10390506 C>G maps to NM_198464.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr8:10387041 G>A maps to NM_198464.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:10383124 G>A maps to NM_198464.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:55970145 C>T maps to NM_173814.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr19:847956 G>A maps to NM_002777.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:79465455 C>A maps to NM_015225.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:79320493 T>G maps to NM_015225.2 A2232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:79324804 C>A maps to NM_015225.2 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:79322997 C>A maps to NM_015225.2 E1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr9:79325135 G>C maps to NM_015225.2 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:79441637 A>G maps to NM_015225.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr19:40903373 C>A maps to NM_181882.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:40903751 G>A maps to NM_181882.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:40902215 G>C maps to NM_181882.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:80921339 G>T maps to ENST00000421149 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr10:104176759 G>A maps to NM_002779.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr10:104170856 C>A maps to NM_002779.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:104172151 C>T maps to NM_002779.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:104164662 G>A maps to NM_002779.3 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr10:104171505 G>A maps to NM_002779.3 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr5:139193043 C>T maps to NM_032289.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr8:18730070 G>A maps to ENST00000440756 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr8:18457933 T>C maps to ENST00000440756 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr2:113943637 C>A maps to NM_012455.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:113940806 G>A maps to NM_012455.2 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr14:73653559 G>C did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr14:73685864 C>T maps to NM_000021.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:43575977 G>A maps to NM_031246.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:43579568 C>A maps to NM_031246.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:43243197 G>T maps to NM_021016.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:43698610 G>C maps to NM_002780.3 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr19:43699231 C>T maps to NM_002780.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:43699168 G>A maps to NM_002780.3 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:43680142 G>A maps to ENST00000270059 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:43430856 T>A maps to NM_002783.2 K241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:43430141 G>A maps to NM_002783.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:43258690 G>T maps to NM_182707.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr19:43766117 G>C maps to NM_002784.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr16:67943530 C>T maps to NM_006742.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr8:87076588 C>A maps to ENST00000276616 G153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr8:87076469 A>G maps to ENST00000276616 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr8:87081731 G>T maps to ENST00000276616 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr18:23759081 T>C maps to NM_144662.2 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr18:23731820 G>T maps to NM_144662.2 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr18:23772371 C>G maps to NM_144662.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr16:67968567 G>A maps to NM_002801.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:151372950 C>T maps to NM_002796.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:23502793 G>A maps to NM_002797.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr6:32810866 C>A did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr11:47444132 G>A maps to NM_002804.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:231951877 T>C maps to NM_002807.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:231937099 G>T maps to NM_002807.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:107334726 T>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:30791090 G>T maps to NM_002815.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr17:65353487 C>T maps to NM_002816.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr2:162242082 G>C did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr3:184020466 G>T maps to NM_002808.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr3:184024267 C>T maps to NM_002808.3 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr17:38142892 C>G maps to NM_002809.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr17:38152591 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:151239681 G>T maps to ENST00000368881 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:64004610 G>C maps to ENST00000492933 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:24612868 C>T maps to ENST00000429021 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:54175568 A>G maps to NM_014614.2 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr2:54147370 G>C maps to NM_014614.2 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:54164583 A>G maps to NM_014614.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:1145090 C>T maps to NM_006814.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr18:12703144 C>A maps to NM_020232.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:56079529 G>A maps to NM_004577.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:28476842 C>T maps to NM_001164721.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:97272494 T>C maps to ENST00000370197 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr7:99022624 G>C maps to NM_001198879.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr2:86361472 C>A maps to NM_017952.5 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:45292237 C>A maps to NM_003738.4 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:45293549 G>A maps to NM_003738.4 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:45291981 G>A maps to NM_003738.4 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:23398341 T>C did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:23398077 A>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:23398155 T>A did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:23397916 C>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:23411488 G>A did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:23411777 G>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:23410787 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:11584056 G>A maps to NM_020780.1 K807K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:11595631 G>A maps to NM_020780.1 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:11596392 C>T maps to NM_020780.1 Q1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:11577557 C>T maps to NM_020780.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr1:11595161 C>G maps to NM_020780.1 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:11589693 C>A maps to NM_020780.1 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:27702763 C>T maps to NM_001034842.3 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:27702887 C>A maps to NM_001034842.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr10:27688068 C>T maps to NM_001034842.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr10:27703065 C>G maps to NM_001034842.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr10:27703180 G>C did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:42883812 C>T maps to NM_138296.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr8:97316351 C>T maps to NM_014754.1 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:97316270 C>T maps to NM_014754.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:490428 A>G maps to NM_030783.1 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr10:89717677 G>T maps to NM_000314.4 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr10:89720807 T>A maps to NM_000314.4 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr10:89725054 C>G maps to NM_000314.4 Y346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr10:89717707 C>T maps to NM_000314.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr10:89685280 C>G maps to NM_000314.4 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr10:89717707 C>T maps to NM_000314.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr10:16526709 G>T maps to NM_030664.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr14:52735260 T>C maps to NM_000953.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:52735194 C>T maps to NM_000953.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:71512399 G>T maps to ENST00000354608 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:40681541 C>T maps to NM_000958.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr9:130885220 G>C maps to NM_025072.5 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr9:130889720 C>A maps to NM_025072.5 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:47126729 G>A maps to NM_000960.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr20:48164499 C>T maps to NM_000961.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr1:186648496 G>A maps to NM_000963.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:13514119 C>T maps to NM_000315.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:209358351 G>T maps to NM_005048.2 G541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr8:141716271 G>A maps to NM_005607.4 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:141799600 G>T maps to NM_005607.4 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr8:27315845 G>T maps to NM_004103.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:43126658 A>G maps to NM_002821.3 R942R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:43111278 C>T maps to NM_002821.3 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr7:136938274 C>T maps to NM_002825.5 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:136939654 G>A maps to NM_002825.5 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr19:50357724 C>T maps to NM_017432.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:17641302 G>A maps to NM_014241.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr10:17636216 T>C maps to NM_014241.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr12:112915506 A>G maps to ENST00000392596 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr12:112893783 G>T maps to ENST00000392596 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:77210754 C>T maps to NM_002835.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr4:87706381 A>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:87695597 C>T maps to NM_080685.2 Q1813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:87671972 G>T maps to NM_080685.2 G1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:214531327 G>A maps to NM_005401.4 I1167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:214556842 T>A maps to NM_005401.4 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:114381217 C>A maps to NM_015967.5 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:47452147 C>T maps to NM_015466.2 Q954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr9:112151659 C>T did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr9:112182804 G>A maps to NM_002829.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:120684189 C>T maps to NM_002830.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:120720313 C>T maps to NM_002830.2 N801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr1:202128421 G>A maps to ENST00000309017 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:70946554 A>G did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr12:70964992 A>G maps to NM_001109754.1 N1061N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:70953210 T>C maps to NM_001109754.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr12:71029759 G>A maps to NM_001109754.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:71029667 G>T maps to NM_001109754.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:70983912 C>T maps to NM_001109754.1 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr12:70986092 C>G maps to NM_001109754.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:198687415 A>G maps to ENST00000271610 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr1:198721754 A>G maps to ENST00000271610 Q1121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:198678942 A>C maps to ENST00000271610 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:8486185 T>C maps to NM_002839.3 E877E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:8497240 C>A did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr9:8319962 C>T maps to NM_002839.3 A1846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr9:8633315 C>T did not map to a codon.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr9:8486188 T>C maps to NM_002839.3 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:44019607 C>G maps to NM_002840.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:44069849 G>T maps to NM_002840.3 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:44070952 G>T maps to NM_002840.3 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:44072011 G>A maps to NM_002840.3 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:44056823 C>T maps to NM_002840.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr3:62216896 A>G did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:55713427 G>T maps to NM_002842.3 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:55715297 A>T maps to NM_002842.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr11:48149572 G>C maps to NM_002843.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr11:48164468 A>G did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr6:128540113 G>C maps to ENST00000368210 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:128411137 C>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr18:8394533 G>T maps to NM_001105244.1 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr18:8113591 G>A maps to NM_001105244.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr18:8069964 G>T maps to NM_001105244.1 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr18:8088777 A>T maps to NM_001105244.1 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:220156189 A>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:220159713 G>T maps to NM_002846.3 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:220161833 C>A maps to NM_002846.3 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:220167144 G>T maps to NM_002846.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:220161193 G>A maps to NM_002846.3 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:220161199 C>T maps to NM_002846.3 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr2:220167081 A>G maps to NM_002846.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:157959908 G>A maps to NM_002847.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr7:157926394 C>T maps to NM_002847.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:157396692 C>T did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:15704491 G>A maps to NM_030667.1 E815E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:15747917 G>A maps to NM_030667.1 K1198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr12:15702146 C>A maps to NM_030667.1 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr12:15650233 A>C maps to NM_030667.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:71286539 C>A maps to NM_002849.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:40747042 C>T maps to ENST00000373198 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr20:40944488 G>T maps to ENST00000373198 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:40713385 G>A maps to ENST00000373198 R1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr20:40710637 C>A maps to ENST00000373198 G1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:40980733 G>T maps to ENST00000373198 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr20:41306583 G>A maps to ENST00000373198 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr20:41419867 G>T maps to ENST00000373198 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:40735488 C>A maps to ENST00000373198 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr20:40713431 G>T maps to ENST00000373198 A1364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr20:40733285 C>A maps to ENST00000373198 E1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:29647243 G>A maps to NM_005704.4 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr1:29609185 A>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:121668636 G>T maps to NM_002851.2 E1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr7:121651115 C>T maps to NM_002851.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:121652897 T>C maps to NM_002851.2 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:121684483 T>G maps to NM_002851.2 Y1982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:40556971 C>A maps to NM_012232.5 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:31437698 G>A maps to ENST00000373741 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:31465306 G>C maps to ENST00000373741 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:20508287 G>A maps to ENST00000361078 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr8:30889971 C>A maps to NM_013357.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr12:132428115 C>T maps to NM_025215.5 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr12:132425924 G>T maps to NM_025215.5 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:105099693 T>C maps to NM_019042.3 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr19:45368681 T>C maps to NM_001042724.1 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:45375119 G>A maps to NM_001042724.1 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:1648442 G>A maps to NM_012293.1 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr2:1680796 G>A maps to NM_012293.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:1680757 C>A maps to NM_012293.1 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:1653433 G>A maps to NM_012293.1 N706N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr2:1653367 G>A maps to NM_012293.1 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:1667511 G>T maps to NM_012293.1 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:52321426 G>A maps to NM_144651.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr8:52323843 C>T maps to NM_144651.4 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr8:52320766 G>C maps to NM_144651.4 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:52322095 G>A maps to NM_144651.4 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr8:52366244 G>T maps to NM_144651.4 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:52384805 G>A maps to NM_144651.4 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:52322089 G>C maps to NM_144651.4 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr8:52321168 C>A maps to NM_144651.4 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr8:52387661 C>T maps to NM_144651.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:52320772 C>T maps to NM_144651.4 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr12:133272598 C>T maps to NM_018663.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:32298405 G>A maps to NM_007238.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:120653416 G>A maps to NM_001080855.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:51378991 C>A maps to NM_002863.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr14:51398404 G>A maps to NM_002863.4 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:64521494 C>A maps to NM_005609.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:64517933 A>G maps to NM_005609.2 N697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr11:64525758 C>A maps to NM_005609.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr15:55838973 G>A maps to NM_015617.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr15:55838298 G>T maps to NM_015617.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr15:55838814 A>G maps to NM_015617.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:154932142 C>T maps to NM_138300.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:158914790 C>T maps to NM_152501.3 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:158908928 G>A maps to NM_152501.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr12:9304821 T>C maps to NM_002864.2 V1402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:9316786 A>G maps to NM_002864.2 Y852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:9356369 G>C maps to NM_002864.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:9313701 C>G maps to NM_002864.2 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:9304845 A>G maps to NM_002864.2 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr12:9349035 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:17513586 G>T maps to NM_000320.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:163899888 C>T maps to ENST00000361752 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr6:163956075 C>T maps to ENST00000361752 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:37586829 C>T maps to NM_012413.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:46205164 C>G maps to NM_017659.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:46206204 C>G maps to NM_017659.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr4:122301678 C>A maps to NM_198179.2 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr4:122301658 G>C maps to NM_198179.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr11:32956814 C>T maps to NM_001076786.1 G1208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:32975555 C>G maps to NM_001076786.1 S1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:32997981 G>T maps to NM_001076786.1 G1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:180166159 C>T maps to NM_002826.4 H744H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:180163489 C>T maps to NM_002826.4 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:180163471 C>T maps to NM_002826.4 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr9:139103152 G>A maps to NM_181701.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr19:10822891 G>A maps to NM_031209.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:10812666 C>T maps to NM_031209.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr3:113804604 C>T maps to ENST00000485050 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr2:136432939 G>T maps to ENST00000409606 G697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr12:57663633 C>T maps to ENST00000438036 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr12:57662126 C>T maps to ENST00000438036 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:26350783 G>A maps to NM_016131.4 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr8:37729088 C>A maps to NM_001002814.2 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr8:37756794 G>T maps to NM_001002814.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr8:37734975 G>T maps to NM_001002814.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:37732085 C>A maps to NM_001002814.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr2:73303201 G>C maps to NM_015470.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr18:8609898 G>C maps to NM_001025300.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr18:8624945 C>T maps to NM_001025300.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:153958589 G>T maps to NM_002870.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr9:123945597 C>A maps to NM_016322.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:65316075 C>T maps to NM_004161.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:72167785 C>T maps to NM_014999.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:72176355 A>T maps to NM_014999.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr6:57075139 C>A maps to NM_016277.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr15:55520834 T>C maps to NM_183235.1 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:55516100 G>T maps to NM_183235.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr4:13370214 G>A maps to NM_001017979.2 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:129318483 C>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr4:140393856 A>T maps to NM_031296.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr17:27043982 C>T maps to NM_001144943.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:27042863 C>A maps to NM_001144943.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:87908498 C>A maps to NM_022337.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:154490469 A>C did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:154493443 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:18313412 C>A maps to NM_002866.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:52399037 C>A maps to NM_002867.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:57913582 T>C maps to NM_138453.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:11447868 C>T maps to NM_004283.3 K69K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-66-2786-01A-01D-1522-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:220384316 G>A maps to ENST00000358951 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:70206563 T>C maps to NM_175623.2 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:102755197 T>C did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:102755637 T>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:102192748 C>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:102192997 G>T did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr17:80618871 C>A maps to NM_006822.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:69502419 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:69502121 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr1:28920445 C>T maps to NM_001193532.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr12:56384545 G>A maps to NM_002868.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr11:73388999 G>A maps to NM_198896.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:133560495 C>T maps to NM_016577.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:13727077 C>T did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:13727146 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:28925736 G>A maps to NM_024816.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:28922460 C>A maps to NM_024816.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:174363265 C>T maps to NM_014857.3 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:174188303 C>T maps to NM_014857.3 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr1:174340114 A>G did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:174190148 G>T maps to NM_014857.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr7:66273904 C>T maps to ENST00000451741 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr7:66270166 G>A maps to ENST00000451741 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:120461342 C>A maps to NM_173825.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:120417268 C>A did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr3:120461338 G>T maps to NM_173825.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr22:37628864 G>C maps to NM_002872.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr22:37627421 T>C maps to NM_002872.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr12:50387973 G>A maps to NM_013277.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:34908870 C>G maps to NM_002853.3 *283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr5:68677864 C>T maps to NM_133339.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:8940592 G>T maps to NM_020165.3 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr8:117869512 T>C maps to NM_006265.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:131915104 C>T maps to NM_005732.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:1038999 C>A maps to NM_134424.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:95412501 T>C maps to NM_012415.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:95416345 T>C maps to NM_012415.2 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:67160216 T>G maps to NM_004584.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:67164769 C>A maps to NM_004584.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr7:4839815 G>A maps to NM_018059.4 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr7:4917590 C>A maps to NM_018059.4 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr7:4917518 G>A maps to NM_018059.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr7:4917419 G>A maps to NM_018059.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr20:55948589 A>T maps to NM_001015885.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr20:55953066 A>G did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr6:150239491 G>T maps to NM_001001788.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr3:12653510 G>C maps to ENST00000415519 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:36595983 C>G maps to NM_000448.2 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:36595198 G>T maps to NM_000448.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr17:17700659 G>A maps to ENST00000395776 R1466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr5:34814734 G>T maps to NM_001145521.1 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:34811910 C>T maps to NM_001145521.1 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:34796082 C>G maps to NM_001145521.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr5:34823167 A>G maps to NM_001145521.1 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr23:17819467 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:17818857 C>A did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:17820020 G>T did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr7:39729979 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:39745753 G>T maps to NM_005402.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr18:9535925 G>A maps to NM_006788.3 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr14:36140705 G>A maps to NM_194301.2 I1191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:20621384 T>A maps to NM_020343.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr20:20486104 C>A maps to NM_020343.3 E1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:37146531 C>A maps to NM_020336.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr20:37146563 C>G maps to NM_020336.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr20:37126040 G>A maps to NM_020336.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr20:37154045 G>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:37169682 G>C did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr8:85785582 C>T maps to NM_001100391.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:85441618 C>A maps to NM_001100391.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:131359124 G>T maps to ENST00000392369 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:67768870 G>A maps to NM_020850.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:67763246 C>A maps to NM_020850.1 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:170323061 G>A maps to NM_022897.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:170692727 C>T maps to NM_022897.3 I940I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr5:170725834 A>G maps to NM_022897.3 E1080E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:109383852 G>A maps to NM_006267.4 Q2286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:109383183 C>G maps to NM_006267.4 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:109347289 T>C maps to NM_006267.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:109384286 C>A maps to NM_006267.4 S2431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:5923309 G>A maps to NM_007322.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr5:36257554 C>T did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr9:6015054 A>G maps to NM_012416.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr6:13632622 A>T maps to NM_005493.2 T642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr22:41670654 C>T maps to NM_002883.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr1:21934780 G>T maps to NM_001145658.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr4:99342541 A>T maps to NM_001100426.1 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr13:98086846 C>T maps to NM_021033.6 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr4:160235906 A>T maps to NM_014247.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:48131350 C>T maps to NM_001098531.2 *924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr12:48142236 C>A maps to NM_001098531.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:173891403 A>G maps to NM_007023.3 E786E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:130828460 G>A maps to ENST00000514667 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:204305806 C>A maps to ENST00000374493 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr2:204305814 G>A maps to ENST00000374493 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr17:38510741 C>T maps to NM_001145301.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:86633841 G>A maps to NM_002890.1 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:86672322 C>T maps to NM_002890.1 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr5:86672712 G>T maps to NM_002890.1 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:86679527 A>G did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr5:86685300 C>G maps to NM_002890.1 S1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:141295905 C>G maps to ENST00000452898 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:114817533 G>A maps to ENST00000389544 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr13:114781702 C>T maps to ENST00000389544 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr12:113539712 G>A maps to NM_001193520.1 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr12:113544951 G>C maps to NM_001193520.1 S537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:178425845 C>A maps to ENST00000263528 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:178427448 C>T maps to ENST00000263528 Q997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr1:178427315 G>A maps to ENST00000263528 K952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:178252762 G>C maps to ENST00000263528 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:15572070 C>A maps to NM_022904.1 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:15574962 C>A maps to NM_022904.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:15565327 C>T maps to NM_022904.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:15572071 G>T maps to NM_022904.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:15564028 C>T maps to NM_022904.1 W853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:15575155 G>T maps to NM_022904.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr22:35943062 C>G maps to NM_014310.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:85607850 G>A maps to NM_152573.2 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:85619502 T>A did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr10:43695153 C>G maps to ENST00000374459 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:79323818 G>A maps to NM_002891.4 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:79323848 G>A maps to NM_002891.4 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr15:79339152 C>G maps to NM_002891.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr15:79339107 G>A maps to NM_002891.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr15:79298688 G>T maps to NM_002891.4 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr15:79298628 G>C maps to NM_002891.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:79339218 C>T maps to NM_002891.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:79290511 G>T maps to NM_002891.4 I980I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr15:79291168 T>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:80476039 G>A maps to NM_006909.1 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:80408536 A>G maps to NM_006909.1 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr5:80515597 G>C did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr15:38794622 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:33749498 A>T maps to NM_170672.2 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:33784045 G>A maps to NM_170672.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr19:38911760 G>C maps to ENST00000405332 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr4:53728715 C>G maps to NM_023940.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:45486417 C>T maps to NM_032023.3 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr10:45486408 A>G maps to NM_032023.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:562243 C>G maps to NM_003475.3 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr12:26218103 G>A maps to NM_001164747.1 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:86199571 C>T maps to NM_005447.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr12:86199108 C>A maps to NM_005447.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:10432271 G>C maps to NM_133452.2 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr18:56939712 C>A maps to NM_013435.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr13:48916732 A>G did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr13:48916851 T>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr13:49030425 C>G maps to NM_000321.2 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr13:49030451 A>T maps to NM_000321.2 K643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr13:48953727 A>G did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr8:53573546 T>C maps to NM_014781.4 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr8:53586628 T>A maps to NM_014781.4 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr8:53568565 A>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr8:53573531 T>C maps to NM_014781.4 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:5105000 C>T maps to NM_021163.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr7:5105027 A>G maps to NM_021163.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:205068919 G>A maps to NM_005057.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:205064079 G>C maps to NM_005057.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr16:24583480 C>G maps to NM_006910.4 V1698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr23:16881152 G>A did not map to a codon.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr18:20573508 A>G maps to ENST00000360790 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr20:18474618 C>T maps to NM_006606.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr20:18470557 G>A maps to NM_006606.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr20:409638 G>A maps to NM_031229.2 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:28050573 C>A maps to NM_022128.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr16:53515705 C>A maps to NM_005611.3 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:47044724 A>G did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr21:15591903 G>C maps to NM_144770.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:34241816 T>C maps to NM_001198838.1 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:94746676 G>A maps to NM_203390.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:110884309 C>A maps to NM_022768.4 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:155116179 C>G maps to NM_014892.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr6:155152161 C>A maps to NM_014892.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr6:155153568 C>T maps to NM_014892.3 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:6155485 C>G maps to NM_001145547.1 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr12:114397944 G>T maps to NM_016196.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr14:73550248 A>T maps to NM_021239.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr13:79940804 C>T maps to ENST00000438737 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr13:79979846 G>C maps to ENST00000438737 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr13:79946000 G>C maps to ENST00000438737 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:48433598 G>T did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr7:155471375 C>T maps to NM_053043.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr11:66411413 A>T maps to NM_001198845.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:106331792 C>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:36122094 C>T maps to NM_024321.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr2:178990746 A>G maps to ENST00000456670 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr2:178988912 A>G maps to ENST00000456670 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:50153356 C>T maps to NM_005778.2 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:50114515 C>T maps to NM_005777.2 R1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:114271398 G>T maps to NM_016090.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr22:36177729 C>A maps to NM_001082578.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr2:161141534 G>T maps to NM_016836.3 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:161133861 G>A maps to NM_016836.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:135958789 A>G did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:135958740 T>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:135956577 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:135961271 C>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:135958711 C>G did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:135960085 C>T did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:129545363 C>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:7110611 G>C maps to NM_014469.4 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:139172002 C>A maps to NM_004164.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:139173595 C>T maps to NM_004164.2 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:48390115 C>T maps to NM_002900.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr10:48389920 G>T maps to NM_002900.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:48389545 G>A maps to NM_002900.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr10:95351848 C>A maps to NM_006744.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:7281009 G>A maps to NM_031491.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:30332341 G>T maps to NM_001008712.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr1:173962057 G>A maps to NM_172071.2 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:125613660 C>A maps to NM_001100588.1 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr13:49085986 G>A maps to NM_001268.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr11:32118818 T>C maps to NM_002901.2 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr11:32118746 G>C maps to NM_002901.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:103177272 G>T maps to NM_015156.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:211654706 G>A maps to NM_183059.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:68151841 C>T maps to NM_016026.3 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:55558803 C>A maps to NM_001145971.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:57346752 C>A maps to NM_003708.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr12:57348691 G>C maps to NM_003708.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:56118298 C>T maps to NM_002905.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr19:10132323 C>A maps to NM_015725.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:36087892 T>C maps to NM_021111.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:36100326 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:145737344 C>T maps to ENST00000428558 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr8:145736870 C>G maps to ENST00000428558 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:79348016 G>A maps to NM_002909.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:79347992 T>A maps to NM_002909.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:79350272 G>C did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:79349974 C>A maps to NM_002909.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:79312343 A>T maps to NM_006507.3 *167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:79313627 G>T maps to NM_006507.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr2:79386510 C>A maps to NM_138937.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:79385463 A>G maps to NM_138937.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:79385531 C>A maps to NM_138937.2 G85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:79255401 G>A maps to NM_001008387.1 *176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:79254171 A>T maps to NM_001008387.1 K70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:79254997 G>A maps to NM_001008387.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:79255036 T>A maps to NM_001008387.1 C146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr2:79254168 C>T maps to NM_001008387.1 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr1:120342440 G>T maps to NM_032044.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:120342481 C>A maps to NM_032044.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:65422460 G>T maps to NM_021975.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr5:141019703 G>T maps to NM_173828.4 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:103123324 G>A maps to ENST00000428762 V3425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:103322648 G>A maps to ENST00000428762 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr7:103191530 C>T maps to ENST00000428762 G2095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr7:103124173 G>A maps to ENST00000428762 I3369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:103205998 C>A did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr7:103206704 A>G maps to ENST00000428762 S1634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:103143677 C>G did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:103159906 G>A maps to ENST00000428762 I2575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:103293014 C>A maps to ENST00000428762 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr7:103206770 G>A maps to ENST00000428762 G1612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:103237090 C>A maps to ENST00000428762 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:103252102 C>T maps to ENST00000428762 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:73105575 C>G maps to NM_152222.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:30070203 C>A maps to NM_014012.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr20:30071998 C>T maps to NM_014012.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:204131206 G>A maps to NM_000537.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:153209165 A>C did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:153209818 G>T did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr23:153207087 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr7:150069553 C>T maps to NM_001099695.1 C465C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr7:150069611 G>T maps to NM_001099695.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:17043188 C>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:17072969 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:8418355 G>A maps to NM_012102.3 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:8525993 C>T maps to NM_012102.3 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:57797661 C>T maps to NM_005612.4 Q880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr4:57796298 G>A maps to NM_005612.4 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:43615123 C>T maps to NM_020975.4 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr3:108475981 C>T maps to NM_032579.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:108475935 T>A maps to NM_032579.2 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr2:100055627 C>T maps to NM_016316.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr6:111694286 T>A maps to NM_002912.3 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:111634623 C>T maps to NM_002912.3 Q2845Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:111634599 T>C maps to NM_002912.3 K2853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:111737631 G>C maps to NM_002912.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:1820349 G>A maps to NM_020695.3 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr9:136272166 C>A maps to NM_020385.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:186512449 G>C maps to NM_181573.2 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr12:118464746 C>A maps to NM_007370.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr22:29837975 C>A maps to NM_021026.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr22:32587045 C>A maps to NM_001098527.2 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr22:32598390 G>T maps to NM_001098527.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr22:32587175 G>A maps to NM_001098527.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr22:32756324 C>T maps to NM_001098535.1 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:112671662 A>G maps to NM_001013734.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:112671179 C>G maps to NM_001013734.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:198498589 T>A maps to NM_144629.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:176133016 G>T maps to NM_022457.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:175958604 G>C maps to NM_022457.5 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr16:74670476 T>G did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:14080948 G>A maps to NM_002918.4 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr9:3330504 C>A maps to NM_134428.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:3277415 T>G maps to NM_134428.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr12:107103137 G>A maps to ENST00000357881 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr12:107080754 C>A maps to ENST00000357881 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:117237247 G>A maps to NM_173560.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr6:117246637 T>A maps to NM_173560.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:117198458 G>T maps to NM_173560.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr6:117240429 C>T maps to NM_173560.3 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr6:117245952 A>G maps to NM_173560.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr15:56385971 G>C maps to NM_022841.5 T1318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr15:56386133 T>C maps to NM_022841.5 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr15:56387338 C>A maps to NM_022841.5 E863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:19308354 C>T maps to NM_003721.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:101283907 A>T maps to NM_017819.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:109694757 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:109694722 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:109697127 C>T did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr23:109694516 C>G did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr23:109694616 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:109697269 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:109696914 T>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:109694326 C>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:109695277 C>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:109696543 C>A did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr23:109694806 C>G did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:109694823 G>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:109694589 G>C did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:109694560 C>G did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:109694196 A>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:71350436 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:71351266 C>A did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:71350234 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:71349716 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:183852929 C>T maps to NM_015149.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:33262479 G>A maps to NM_004761.3 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:11515846 G>C maps to NM_001161616.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr19:11527688 G>A maps to NM_001161616.1 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:11510614 C>T maps to NM_001161616.1 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr19:11527292 G>A maps to NM_001161616.1 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:24034554 C>A maps to ENST00000382833 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr15:93588838 T>A maps to NM_020211.2 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:73069771 C>T maps to NM_001080479.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr5:73163737 C>T maps to NM_001080479.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr2:87214093 A>T maps to NM_001078170.2 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:86012760 G>A maps to ENST00000358110 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr10:86017683 C>A maps to ENST00000358110 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:192547368 G>T maps to NM_002922.3 G100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:121285579 T>C maps to NM_001005339.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr4:3318113 A>T maps to NM_198229.2 K73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:3418747 C>T maps to NM_198229.2 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr4:3318705 C>A maps to NM_198229.2 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:3427267 G>A maps to NM_198229.2 K1104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:192150518 A>T maps to NM_130782.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:54791981 C>T maps to NM_170587.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr8:101052291 A>C maps to NM_015668.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr8:100994302 C>T maps to NM_015668.3 K1074K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:163044271 G>A maps to NM_001102445.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:163138132 C>A maps to NM_003617.3 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:163138097 G>A maps to NM_003617.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:163117133 A>G maps to NM_003617.3 *182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr14:72943475 C>T maps to NM_004296.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:240966239 G>T maps to ENST00000407727 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:241146394 T>C maps to ENST00000407727 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:241099905 C>G maps to ENST00000407727 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:240978013 A>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:240939491 T>G maps to NM_002924.4 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:240966245 T>A maps to ENST00000407727 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:241099991 A>G maps to ENST00000407727 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:63905036 G>A maps to NM_001029875.1 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:63193339 C>T maps to NM_003835.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:63193282 C>A maps to NM_003835.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:63185417 T>C maps to NM_003835.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:63221469 G>C maps to NM_003835.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr17:63198195 C>A maps to NM_003835.3 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:33167780 G>T maps to NM_207391.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:49578735 C>T did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr6:49578735 C>T did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr6:49582416 G>A maps to NM_000324.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:49582402 G>A maps to NM_000324.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:49582567 T>C did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:49604510 G>A maps to NM_000324.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr16:111618 C>A maps to NM_022450.3 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr16:111893 C>A maps to NM_022450.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:74473788 C>A maps to NM_024599.5 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:74475253 C>T maps to NM_024599.5 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr17:74476008 C>T maps to NM_024599.5 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:74473801 C>T maps to NM_024599.5 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:726322 C>T maps to NM_003961.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:30611718 C>T maps to NM_138328.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr17:30621461 G>C did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:156352619 T>C maps to NM_020407.3 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:156347188 C>T maps to NM_020407.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:25715487 G>A maps to NM_020485.4 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:25617254 G>A maps to ENST00000357542 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:25628017 C>G maps to ENST00000357542 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:25627435 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr12:49460813 G>C maps to NM_144593.1 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:129249755 C>T maps to NM_000539.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr3:129247866 C>A maps to NM_000539.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:129251163 G>T maps to NM_000539.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr10:62648180 G>C maps to NM_014836.4 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:40245212 G>A maps to NM_004310.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:63749906 C>A maps to NM_020663.3 Y157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr14:63747705 G>T maps to NM_020663.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:46803779 G>A maps to NM_012249.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr17:30519305 C>A maps to NM_001033568.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr17:30521102 G>A maps to NM_001033568.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr16:723527 G>T maps to NM_138769.1 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:119249578 C>T did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr8:144463804 C>A maps to ENST00000422773 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:144461551 C>T maps to ENST00000422773 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:33490525 G>A maps to NM_033103.4 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:53455273 G>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:107236522 C>A maps to ENST00000392837 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr5:38963106 G>A maps to ENST00000296782 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:38962426 G>A maps to ENST00000296782 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr5:38960532 G>A maps to ENST00000296782 C606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:152325192 A>G maps to NM_018151.4 T2288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:152300041 G>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:152319635 C>G maps to NM_018151.4 S1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:123970352 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:130941080 G>A maps to NM_015347.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr12:130919365 G>A maps to NM_015347.4 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:130892300 G>T maps to NM_015347.4 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:130884262 G>A maps to NM_015347.4 H1031H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:130935769 G>A maps to NM_015347.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr12:8926043 C>G maps to NM_020734.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:72957739 G>A maps to NM_014989.4 Q717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr6:72975122 A>G maps to NM_014989.4 K1075K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr6:72957821 C>T maps to NM_014989.4 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr6:73000537 G>A maps to NM_014989.4 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:72806702 G>A maps to NM_014989.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:73102501 C>A maps to NM_014989.4 T1536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr6:72967966 A>T maps to NM_014989.4 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:72892797 G>T maps to NM_014989.4 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:72960792 G>T maps to NM_014989.4 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:105261766 C>T maps to NM_001100117.2 I1214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr8:105263841 G>T maps to NM_001100117.2 G1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr8:104898413 T>C maps to NM_001100117.2 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr20:19945644 C>G maps to ENST00000255006 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr14:93118173 C>T maps to NM_024832.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr14:93107666 G>T maps to NM_024832.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr14:93043794 G>T maps to NM_024832.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:33179273 G>C maps to NM_002931.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr19:39361378 G>A maps to NM_001195833.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr7:105177042 T>C maps to NM_021930.4 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr5:96514780 G>C maps to NM_018343.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr18:21059300 C>G maps to NM_003831.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr21:43161627 G>A maps to ENST00000352483 H623H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr21:43161624 G>T maps to ENST00000352483 Y624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr21:43161930 C>A maps to ENST00000352483 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr21:43164075 C>A maps to ENST00000352483 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr21:43161306 G>A maps to ENST00000352483 H730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr6:84563452 C>T maps to NM_001009994.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr18:40503644 T>A maps to NM_002930.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr18:40695400 T>C maps to NM_002930.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:40701551 C>G maps to NM_012421.3 S393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr23:73812014 C>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:73811972 C>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:73812545 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:73811706 G>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:73812558 T>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:73812707 C>G did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr9:5300280 G>C maps to NM_134441.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:14141726 G>C maps to NM_080864.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr19:14139150 C>T maps to NM_080864.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr16:67683723 C>T maps to NM_001013838.1 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:67688559 G>T maps to NM_001013838.1 E1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr9:86616458 C>T maps to NM_024945.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:177573149 C>A maps to NM_022762.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr14:21269780 A>G maps to NM_198235.2 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:20978872 A>G maps to ENST00000430083 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr14:21058510 G>T maps to NM_001024822.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr14:21360007 C>A maps to NM_002935.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:21167598 C>G maps to NM_194431.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:21526419 G>A maps to NM_138331.1 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr17:6916009 C>A maps to NM_001004333.3 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:182554629 C>A maps to NM_021133.3 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:182551333 C>G maps to NM_021133.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:182544527 C>T maps to NM_021133.3 *742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:31526643 G>A maps to NM_013235.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr5:31409193 C>A maps to NM_013235.4 E1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:31508726 C>A did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:31464341 C>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr6:167347620 C>T maps to ENST00000428859 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:151343231 C>A maps to NM_005168.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:59344502 G>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr15:59377921 T>C maps to ENST00000434298 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:119004852 C>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:119005419 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:71706588 C>T maps to NM_018320.4 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:49753119 C>T maps to NM_022064.2 F1041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:49758713 G>T maps to NM_022064.2 T1307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:652862 C>A maps to ENST00000340092 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:105970509 G>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:106031166 A>G did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr7:122338497 T>A maps to NM_139175.1 K159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:7160793 C>T maps to NM_014746.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr5:158621749 G>A maps to NM_144726.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr5:158585995 T>G maps to NM_144726.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:127608135 A>G maps to ENST00000368314 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:101893735 G>A maps to NM_173647.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr18:59483297 C>A maps to NM_173557.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr17:74154523 C>A maps to NM_052916.2 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr21:30302817 T>C maps to NM_015565.2 T1797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr21:30354686 G>A maps to NM_015565.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr21:30304832 G>T maps to NM_015565.2 R1723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr21:30304964 G>T maps to NM_015565.2 R1679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:42729124 T>C maps to NM_030954.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:13977367 T>G maps to NM_001165033.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:20141491 C>A maps to NM_019062.1 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:20141182 C>A maps to NM_019062.1 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr8:101281075 A>C maps to NM_183419.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:101271233 C>A maps to NM_183419.1 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr9:104297791 G>A maps to NM_019592.5 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr9:104317100 G>A maps to NM_019592.5 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr9:104324229 A>G maps to NM_019592.5 T896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:104309490 C>A maps to NM_019592.5 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:6272364 G>T maps to NM_207396.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:78268621 G>A maps to NM_020914.4 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:78272201 G>T maps to NM_020914.4 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:78321521 G>A maps to NM_020914.4 V3178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:78282824 G>T maps to NM_020914.4 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr17:78282824 G>T maps to NM_020914.4 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr17:78355399 G>A maps to NM_020914.4 Q4666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr17:78337587 C>G maps to NM_020914.4 V3965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:78360161 C>T maps to NM_020914.4 V4933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:117150918 G>T maps to NM_207343.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:5769094 C>A maps to NM_207111.2 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:5754761 C>A maps to NM_207111.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr13:79213074 T>A maps to NM_024546.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr13:79216304 C>T maps to NM_024546.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr13:79213125 A>G maps to NM_024546.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:219532649 C>T maps to NM_022453.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:56438266 C>T maps to NM_017763.4 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr17:56435696 G>A maps to NM_017763.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:56434895 C>T maps to NM_017763.4 W747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr3:141464055 G>A maps to NM_014245.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr6:37328290 C>A maps to NM_003958.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:37344704 G>T maps to NM_003958.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:13737114 T>C maps to NM_003799.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr18:13759959 C>G maps to NM_003799.1 A471A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-33-6737-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:685695 G>T maps to NM_018146.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:241515973 C>G maps to NM_018226.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr3:78796019 G>T maps to NM_002941.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:77571934 C>T maps to ENST00000332191 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr3:77147369 C>A maps to ENST00000332191 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr3:77542410 C>G maps to ENST00000332191 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr11:124743725 T>A maps to NM_022370.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:124748010 G>A maps to NM_022370.3 W1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:124748512 T>C maps to NM_022370.3 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr11:124745137 T>A maps to NM_022370.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:124757009 G>A maps to NM_019055.5 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr11:124756582 C>T maps to NM_019055.5 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr11:124766106 C>T maps to NM_019055.5 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr11:124767625 G>A maps to NM_019055.5 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:124757084 G>T maps to NM_019055.5 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:124766100 G>A maps to NM_019055.5 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr18:18533573 G>A maps to NM_005406.2 F1342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr2:11342231 T>G maps to NM_004850.3 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:11426669 G>A maps to NM_004850.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr9:115038168 T>C maps to NM_001163790.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr3:125701207 C>T maps to NM_001012337.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:64644213 G>A maps to NM_005012.2 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:77257577 C>T maps to ENST00000396204 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:151787698 A>T maps to ENST00000392697 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:151786030 C>T maps to ENST00000392697 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:117632190 G>A maps to NM_002944.2 F2075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:117622241 T>A maps to NM_002944.2 R2210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:117710801 G>A maps to NM_002944.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:117678017 G>A maps to NM_002944.2 I1305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr6:117709003 T>A maps to NM_002944.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr6:117706941 G>T maps to NM_002944.2 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr6:117700283 C>A maps to NM_002944.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:117714484 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:55541634 C>T maps to NM_006269.1 I1731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr8:55539798 T>C maps to NM_006269.1 S1119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr8:55541883 A>T maps to NM_006269.1 L1814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr8:55542670 C>T maps to NM_006269.1 Q2077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:55533753 C>A maps to NM_006269.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr8:55534820 G>T maps to NM_006269.1 G254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr8:55537320 T>G maps to NM_006269.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:55541404 C>T maps to NM_006269.1 Q1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr8:55538973 T>A maps to NM_006269.1 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr8:55534011 C>A maps to NM_006269.1 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:55542145 C>T maps to NM_006269.1 Q1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:55541286 C>A maps to NM_006269.1 G1615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:10465664 C>T maps to NM_178857.5 E1981E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:10468420 C>A maps to NM_178857.5 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:10468058 G>A maps to NM_178857.5 D1183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr8:10464902 C>T maps to NM_178857.5 G2235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr8:10466483 C>A maps to NM_178857.5 V1708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr8:10465649 G>A maps to NM_178857.5 T1986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr8:10464584 G>T maps to NM_178857.5 T2341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr17:1783859 A>G maps to NM_002945.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:96139742 T>C did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:96139862 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:41817283 C>A maps to NM_015540.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr15:41827133 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:41822153 G>A maps to NM_015540.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr12:48090171 G>A maps to NM_024604.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:38145004 C>T did not map to a codon.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr23:38145142 C>A did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:38146438 C>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:38144828 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:38146391 C>G did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:38163976 T>C did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:38164002 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr16:53730169 T>C maps to NM_015272.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr12:113307827 C>T maps to NM_001143854.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:113314522 A>G maps to NM_001143854.1 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:89028821 C>A maps to NM_144563.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:88991248 C>G maps to NM_144563.2 Y11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:89049496 G>T did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:153627840 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:153628195 C>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr14:47120930 G>T maps to NM_080746.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr17:27047812 G>A maps to ENST00000394938 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr5:172396423 C>T maps to NM_016093.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr22:39709249 G>A maps to NM_000967.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:99057208 C>A maps to NM_000989.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr4:109543359 G>T maps to NM_033625.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr16:2000846 G>A maps to NM_005061.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr15:66792510 C>T maps to NM_000968.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr15:66793357 T>C maps to NM_000968.2 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr12:112844595 G>A maps to NM_001024662.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr8:146015200 C>T maps to NM_000973.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:146016767 C>T maps to NM_000973.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:146017418 C>A maps to NM_000973.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr10:92631757 A>T maps to ENST00000458617 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:150429814 C>T maps to NM_015203.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr1:150429918 A>T maps to NM_015203.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:34386163 T>A maps to NM_001014.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:42373787 C>T maps to NM_001022.3 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr16:2012181 G>A maps to NM_002952.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr24:2712179 C>T did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr24:22918695 T>G did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr24:22930791 C>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:58906107 C>G maps to NM_001009.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr9:19378868 G>A maps to NM_001010.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr6:166918100 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:20194425 C>A did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:20195155 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64138828 G>A maps to NM_003942.2 K732K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:83390217 C>A did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:83362034 C>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:83371241 A>C did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:83352799 A>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:83419351 T>C did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr23:83320046 A>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:83362665 C>G did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:83319289 G>A did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr11:67201892 C>T maps to NM_003952.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:67202552 G>T maps to NM_003952.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr1:213415137 C>A maps to NM_012424.3 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:54711427 C>T maps to NM_001013.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:152128743 T>A maps to NM_001122965.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:152129160 C>T maps to NM_001122965.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:152128551 G>T maps to NM_001122965.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:152127903 G>T maps to NM_001122965.1 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:152128929 G>T maps to NM_001122965.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:78681765 C>A maps to NM_020761.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr17:78867567 C>T maps to NM_020761.2 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:78921038 G>A maps to NM_020761.2 W1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:9882215 G>T maps to NM_173659.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:219445384 A>T maps to NM_005444.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:219457064 C>T maps to NM_005444.1 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr9:19049818 G>A maps to NM_006570.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:90097268 C>A maps to NM_021244.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr20:17594838 G>A maps to ENST00000377813 G1407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:17610500 C>A maps to ENST00000377813 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:7231820 C>T maps to NM_001003699.3 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr6:7247353 C>T maps to NM_001003699.3 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:6622566 T>A maps to NM_015324.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr3:51967583 G>T maps to NM_004704.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:7036063 G>C maps to NM_080657.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:114308798 T>G maps to NM_018364.3 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:114310947 G>C maps to NM_018364.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:114308979 G>A maps to NM_018364.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr7:77407730 C>T maps to NM_198467.2 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:77325945 C>A maps to NM_198467.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr11:77412452 T>C maps to NM_016578.3 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr11:77412281 T>C maps to NM_016578.3 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr16:11945309 C>A maps to NM_015659.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr16:11933740 A>G maps to NM_015659.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr7:5967998 G>T maps to NM_173565.3 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:116938130 T>C maps to NM_001010892.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr19:46313931 C>A maps to NM_030785.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:46308013 G>A maps to NM_030785.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr6:127476524 A>T maps to ENST00000368317 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr16:57265165 T>G maps to NM_133368.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr16:57243026 T>G maps to NM_133368.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr3:157839906 C>A maps to NM_016625.2 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:158261980 G>T maps to NM_016625.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:122995668 T>C maps to NM_023012.5 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:122991434 C>T maps to NM_023012.5 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr10:16737122 T>A maps to NM_012425.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr10:16858987 C>T maps to NM_012425.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:16796962 G>A maps to NM_012425.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr22:23401852 C>A maps to NM_014433.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr22:23476327 G>A maps to NM_014433.2 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:62326723 C>T maps to ENST00000482936 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr20:62319500 G>A maps to ENST00000482936 E535E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:41770813 C>A maps to NM_015138.4 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:74653635 G>A maps to NM_001015055.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr10:63999435 T>A maps to NM_145307.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:63517541 G>T maps to ENST00000377819 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr2:55253584 C>G maps to NM_020532.4 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr11:57235244 C>T maps to NM_178570.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr3:186917713 C>T maps to NM_153708.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr3:187416620 C>A maps to NM_001004312.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr3:187416660 C>A maps to NM_001004312.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:46541959 C>A maps to NM_031440.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr18:67833308 C>A maps to NM_173630.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr18:67813009 C>T maps to NM_173630.3 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr18:67855445 C>T maps to NM_173630.3 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:70143565 G>A maps to NM_017987.4 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:71672243 G>A maps to NM_001037442.2 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:71650541 G>T maps to NM_001037442.2 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:41143504 G>A maps to NM_173079.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr16:12142232 G>A maps to NM_032167.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr16:12136787 C>G maps to NM_032167.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr7:87370836 C>T maps to NM_138290.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr21:36252917 G>A maps to NM_001754.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr8:93017414 G>T maps to NM_175634.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr6:45480079 C>A maps to ENST00000359524 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr6:45480106 G>A maps to ENST00000359524 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr6:45405762 A>C maps to ENST00000359524 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr6:45514571 G>T maps to ENST00000359524 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:25229098 C>A maps to NM_001031680.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:155292627 C>A maps to NM_001105203.1 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr3:127842516 G>A maps to NM_003707.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr3:127820472 C>A maps to NM_003707.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr19:49507557 C>T maps to NM_006666.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:184570715 C>A maps to ENST00000326397 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr13:32332512 T>C maps to NM_130806.3 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr5:33937195 C>A maps to NM_016568.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr5:33937483 G>T maps to NM_016568.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:155912481 C>A maps to NM_181885.2 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr9:137328330 C>T maps to NM_002957.4 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr9:137300035 C>T maps to NM_002957.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr9:137293517 G>T maps to NM_002957.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:165386446 G>T maps to NM_006917.4 Y151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:165376128 A>G maps to NM_006917.4 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:165386325 G>A maps to NM_006917.4 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:39002949 C>A maps to NM_000540.2 S3100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:38937381 C>T maps to NM_000540.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:38990383 C>T maps to NM_000540.2 A2379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:39062861 G>A maps to NM_000540.2 L4650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr19:38948933 T>C did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr19:38959613 C>A maps to NM_000540.2 R1130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr19:38959967 G>T maps to NM_000540.2 G1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:38980837 C>T maps to NM_000540.2 L1979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr19:39019662 C>T maps to NM_000540.2 L3703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr19:38948828 C>T maps to NM_000540.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:38991552 G>T maps to NM_000540.2 E2513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:237991682 C>T maps to NM_001035.2 L4865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:237729894 C>A maps to NM_001035.2 T1081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr1:237780583 A>C did not map to a codon.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:237806706 C>A maps to NM_001035.2 G2434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:237550609 C>T maps to NM_001035.2 H202H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:237693747 T>C maps to NM_001035.2 C948C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:237758947 A>G maps to NM_001035.2 T1529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:237580423 G>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:237890481 C>T maps to NM_001035.2 P3607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:237711811 G>A maps to NM_001035.2 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:237817614 C>A maps to NM_001035.2 C2622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:237947410 G>T maps to NM_001035.2 L4133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:237947455 C>A maps to NM_001035.2 V4148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:237794790 G>T maps to NM_001035.2 E2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:237730075 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:237778137 T>C maps to NM_001035.2 L1904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:237955580 G>C maps to NM_001035.2 T4580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:237670107 T>C maps to NM_001035.2 Y904Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:237787169 G>T maps to NM_001035.2 G2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:237886495 C>T maps to NM_001035.2 T3541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:237758860 C>G maps to NM_001035.2 R1500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:237936936 G>T maps to NM_001035.2 E3922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:237789105 T>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:237794798 G>A maps to NM_001035.2 V2171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:237949312 C>T maps to NM_001035.2 T4435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr1:237819248 A>G maps to NM_001035.2 E2698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:237604758 G>A maps to NM_001035.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:237817702 C>T maps to NM_001035.2 L2652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr1:237806747 G>C did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:237947188 G>A maps to NM_001035.2 T4059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:237919649 G>A maps to NM_001035.2 A3736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:34047307 G>A maps to NM_001036.3 K2814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr15:34042219 G>A maps to NM_001036.3 W2747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:33872197 C>A maps to NM_001036.3 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr15:34130030 G>A maps to NM_001036.3 G3950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:33954960 C>A maps to NM_001036.3 R1744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:33952003 G>A maps to NM_001036.3 L1464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:33952492 C>G maps to NM_001036.3 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:34023742 C>A maps to NM_001036.3 L2424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:34102747 C>T maps to NM_001036.3 S3365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr15:33858997 C>A maps to NM_001036.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr15:34130642 C>T maps to NM_001036.3 T4154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:33988491 G>T maps to NM_001036.3 L1978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr15:34064312 C>A maps to NM_001036.3 S3003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr15:33999220 C>A maps to NM_001036.3 Y2195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr15:33927920 G>A maps to NM_001036.3 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr15:33938727 G>A did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr15:33999172 C>T maps to NM_001036.3 A2179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:33991933 C>A maps to NM_001036.3 C2093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:34131111 G>T maps to NM_001036.3 E4311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr15:34021226 A>C maps to NM_001036.3 T2401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr15:33922196 A>T maps to NM_001036.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr15:34080534 T>C maps to NM_001036.3 L3236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:34147052 C>T maps to NM_001036.3 I4649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:151955755 C>T maps to NM_002966.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:152006195 A>G maps to NM_005620.1 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:153520928 G>A maps to NM_002960.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:153431477 A>T maps to NM_002963.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:153390677 C>T maps to NM_176823.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:33291858 C>T maps to NM_022753.2 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:101704701 C>T maps to NM_001400.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr1:101704794 C>A maps to NM_001400.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr19:10334966 G>A maps to NM_004230.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:3179146 C>T maps to NM_003775.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:10624742 G>A maps to NM_001166215.1 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:18111803 C>A maps to NM_138421.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:23928926 C>T maps to NM_014363.4 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr13:23909098 T>A maps to NM_014363.4 P2972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr13:23912515 G>T maps to NM_014363.4 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr13:23909194 T>C maps to NM_014363.4 T2940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:5641788 C>T maps to ENST00000433404 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr19:5664450 G>T did not map to a codon.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:5621404 C>T maps to NM_014649.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:134990720 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:134993740 C>A did not map to a codon.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr23:134987409 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:134990766 A>G did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:134994063 G>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:134987550 C>G did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:134989134 C>A did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr23:134987482 C>G did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:134991915 G>A did not map to a codon.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr16:51175079 C>T maps to ENST00000251020 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr16:51175910 T>A maps to ENST00000251020 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr16:51171034 G>T maps to ENST00000251020 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr16:51174482 A>T maps to ENST00000251020 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:51174428 G>C maps to ENST00000251020 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:51175306 G>A maps to ENST00000251020 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr16:51175940 G>A maps to ENST00000251020 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:21993776 C>A maps to NM_005407.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr14:21992790 C>T maps to NM_005407.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr14:21990846 C>T maps to NM_005407.1 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr18:76752542 C>T maps to NM_171999.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr18:76753466 C>T maps to NM_171999.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr18:76752198 C>T maps to NM_171999.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr18:76753967 G>A maps to NM_171999.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr18:76754396 G>A maps to NM_171999.2 E802E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr18:76755005 C>T maps to NM_171999.2 F1005F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr18:76754090 G>T maps to NM_171999.2 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr18:76753664 C>A maps to NM_171999.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:130466547 T>C maps to ENST00000457563 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:130497077 T>G maps to ENST00000457563 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:39866416 C>G maps to NM_018028.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr3:169644859 G>T maps to NM_182610.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr10:76910348 G>A maps to ENST00000372690 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr7:92731246 G>A maps to NM_017654.3 F1388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:92761650 G>A maps to NM_152703.2 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr20:35526236 G>A maps to NM_015474.3 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:128707901 G>A maps to NM_001145928.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:21715093 C>A maps to NM_005870.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:174292540 C>A maps to NM_003864.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:153830691 C>T maps to NM_024632.5 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:55752351 G>A maps to ENST00000443936 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:55743014 G>A maps to ENST00000443936 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr22:50845249 C>A maps to ENST00000216061 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr17:26708233 G>T maps to ENST00000379061 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:109779169 G>A maps to ENST00000369923 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:39412888 C>A maps to NM_017827.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr12:108936866 T>A maps to NM_014706.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:108920091 C>T maps to NM_014706.3 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:148711340 C>T maps to NM_015278.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr6:148855978 G>A maps to NM_015278.3 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr6:148840987 G>T maps to NM_015278.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr23:128925031 G>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:128927641 G>A did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr3:18457566 A>G maps to ENST00000332610 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:18393543 C>G maps to ENST00000332610 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:200193543 G>A maps to NM_001172509.1 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr2:200298127 A>G maps to NM_001172509.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:200193474 A>G maps to NM_001172509.1 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr2:200298193 G>C maps to NM_001172509.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:84362696 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:84362764 A>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:84362448 G>C did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr23:84363063 G>C did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr7:66453477 C>G maps to NM_016038.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr22:50897935 G>A maps to ENST00000337034 V1227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr22:50901146 C>A did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr22:50897989 G>A maps to ENST00000337034 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr22:50885627 G>A maps to ENST00000337034 D1885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr11:10014012 A>G maps to NM_030962.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr11:9861055 T>C maps to NM_030962.3 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:56042608 G>A maps to NM_001101401.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr12:123818602 G>T maps to NM_001167856.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:123800191 G>C maps to NM_001167856.1 S984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:123812521 G>C maps to NM_001167856.1 S450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr19:1108808 C>T maps to NM_014963.2 R1195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:36017689 G>T maps to NM_001166034.1 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:28541121 G>A maps to NM_052923.1 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:28543803 G>A maps to NM_052923.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr6:28542543 A>T maps to NM_052923.1 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:28542453 C>A maps to NM_052923.1 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr6:28543353 T>C maps to NM_052923.1 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:28543071 C>T maps to NM_052923.1 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:47465449 G>A maps to NM_012235.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:47465534 G>T maps to NM_012235.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr15:76673732 G>A maps to ENST00000324767 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:27516289 C>T maps to NM_016240.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr8:27729451 C>A maps to NM_173833.5 *496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:125294742 C>T maps to NM_005505.4 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:1542191 G>A maps to NM_003693.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:1543014 G>C maps to NM_003693.2 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr17:1542991 G>C maps to NM_003693.2 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr10:102116492 G>A maps to NM_005063.4 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr13:78192137 G>A did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr13:78208525 A>T maps to NM_144777.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:53751991 G>C maps to NM_152540.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:224463019 C>T maps to NM_003469.4 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr15:52005587 T>C maps to NM_013243.3 H422H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr15:51984507 T>C maps to NM_013243.3 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:51973990 A>G maps to NM_013243.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:25669791 C>A maps to NM_006998.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr6:25661811 G>T maps to NM_006998.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:12684269 C>G maps to NM_001112706.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:12692274 A>T maps to NM_001112706.2 K695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr4:129867241 G>A maps to NM_144643.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:129809878 C>T maps to NM_144643.2 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:238978059 G>T maps to NM_016510.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr2:238991887 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:18264871 T>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:18259478 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:18283873 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:18259410 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:18283769 G>C did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:18323181 C>G did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:38835282 T>C maps to NM_006514.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr3:38740050 G>A maps to NM_006514.2 L1554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:38798290 C>A maps to NM_006514.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr3:38805034 T>A maps to NM_006514.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:38781047 C>A maps to NM_006514.2 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr3:38805050 T>G maps to NM_006514.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr3:38805038 T>G maps to NM_006514.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:38830445 C>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:38798187 C>A maps to NM_006514.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:38962735 G>C maps to ENST00000302328 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr3:38945399 T>A maps to ENST00000302328 K600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:38938417 C>T maps to ENST00000302328 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:166895998 C>A maps to NM_001165963.1 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:166848152 C>A maps to NM_001165963.1 E1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr2:166915198 C>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr2:166870370 C>A maps to NM_001165963.1 V1196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:166929996 G>A maps to NM_001165963.1 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:166848357 A>G maps to NM_001165963.1 Y1809Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:166866282 C>T maps to NM_001165963.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:166848465 G>A maps to NM_001165963.1 S1773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr2:166848432 G>T maps to NM_001165963.1 V1784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:166892836 T>C maps to NM_001165963.1 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr2:166895937 G>A maps to NM_001165963.1 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:166866245 G>T maps to NM_001165963.1 R1329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:166152500 G>A maps to NM_001040142.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:166188041 G>A maps to NM_001040142.1 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:166201105 T>C maps to NM_001040142.1 N868N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:166165187 A>G maps to NM_001040142.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:166245259 G>T maps to NM_001040142.1 T1648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:166165900 G>C maps to NM_001040142.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:166183443 C>G maps to NM_001040142.1 S700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:166188011 C>A maps to NM_001040142.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:165997166 G>T maps to NM_006922.3 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr2:165970325 C>T maps to NM_006922.3 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:123516381 G>A maps to NM_018400.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr11:123516384 C>G maps to NM_018400.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr17:62018541 G>T maps to NM_000334.4 T1700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr17:62018274 C>A maps to NM_000334.4 S1789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr17:62022728 G>C maps to NM_000334.4 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr17:62049161 C>A maps to NM_000334.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:62036741 G>A maps to NM_000334.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:38645520 G>A maps to NM_001099404.1 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:38616871 C>T maps to NM_001099404.1 L1194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:38639228 G>A maps to NM_001099404.1 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:38601751 G>T maps to NM_001099404.1 I1377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:167319015 A>G maps to NM_002976.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr2:167322347 G>A maps to NM_002976.2 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:167266364 T>C maps to NM_002976.2 Q1264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:52162745 C>A maps to NM_014191.2 S1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:167141025 G>A maps to ENST00000303354 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr2:167141223 G>A maps to ENST00000303354 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr2:167108341 A>T maps to ENST00000303354 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:167141003 G>A maps to ENST00000303354 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr2:167133749 A>G maps to ENST00000303354 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:167133840 G>T maps to ENST00000303354 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:6483595 G>A maps to NM_001159576.1 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr12:6458147 C>T maps to NM_001159576.1 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr16:23391848 C>T maps to ENST00000307331 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:23383104 T>C maps to ENST00000307331 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:1226034 C>G maps to NM_001130413.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:23226586 G>T maps to NM_001039.3 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:53446097 A>T maps to NM_002979.4 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:144890811 C>T maps to NM_182706.3 K694K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr8:144874433 G>T maps to NM_182706.3 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr8:144894453 G>A maps to NM_182706.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:144892669 C>G maps to NM_182706.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr8:144874790 G>A maps to NM_182706.3 Q1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr17:45915973 G>A maps to NM_138355.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:120221812 G>A maps to NM_002980.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:120204406 G>A maps to NM_002980.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:9101051 G>A maps to ENST00000457346 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr6:35214014 C>T maps to ENST00000394681 R945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr12:100729438 G>A maps to NM_017988.4 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr12:100709334 G>T did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:100732316 G>A maps to NM_017988.4 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:20403984 C>T maps to NM_001006946.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr1:243581360 A>G maps to NM_006642.3 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:243504390 G>A maps to NM_006642.3 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr1:1153990 G>A maps to NM_016176.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:231089 A>C maps to NM_004168.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:17345378 A>C maps to NM_003000.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:17371319 G>A maps to NM_003000.2 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:4188934 G>T maps to NM_152744.3 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:4169652 C>G maps to NM_152744.3 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:4089004 G>T maps to NM_152744.3 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:3991403 G>T maps to NM_152744.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr7:4249699 C>T maps to NM_152744.3 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr17:71346875 G>A maps to NM_001144952.1 L1938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:82033638 G>T maps to NM_145168.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:113831700 G>A maps to NM_006843.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr12:113835190 G>A maps to NM_006843.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr12:113874663 T>C maps to NM_138432.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr12:113867082 C>T maps to NM_138432.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr3:10347306 G>A maps to ENST00000343726 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:75210047 G>C maps to NM_001039573.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr22:30818327 G>T maps to NM_012429.2 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr22:30891953 T>A maps to NM_174977.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr16:5053516 C>T maps to NM_014692.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr16:5009368 G>A maps to NM_014692.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:5046872 C>T maps to NM_014692.1 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:5058477 G>T maps to NM_014692.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr9:139369733 C>G maps to NM_014866.1 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:139353939 G>A maps to NM_014866.1 Y1753Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:177906550 C>G maps to NM_033127.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:177913755 C>A maps to NM_033127.2 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:177933401 C>T maps to NM_033127.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:122942493 C>T maps to NM_012430.4 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:145112514 C>A maps to NM_004892.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:145112436 C>A maps to NM_004892.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:145109535 G>A maps to NM_004892.4 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr14:39565183 C>A maps to NM_006364.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr14:39514365 C>A did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr20:18529359 C>T maps to NM_001172745.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr20:18506560 T>C maps to NM_001172745.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:121692596 C>T maps to NM_007190.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr10:121671668 T>C maps to NM_007190.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr10:121658164 G>A maps to NM_007190.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr5:133996854 A>G maps to NM_021982.1 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr4:110415819 A>G maps to NM_006323.2 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:110447380 G>T did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr10:75519789 C>T maps to NM_198597.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr4:119644735 G>A maps to ENST00000379735 Y1012Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:108225922 G>A maps to NM_007214.4 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr15:49329816 G>A maps to NM_001193489.1 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:81956809 C>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:81972507 C>A maps to NM_005065.4 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:13846115 G>A maps to NM_025229.1 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr20:13868587 C>T maps to NM_025229.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr20:13856731 C>T maps to NM_025229.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr4:25821451 G>A maps to NM_015187.3 H467H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:25783962 G>T maps to NM_015187.3 Y786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:169698354 C>T maps to NM_000450.2 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:169696586 G>T maps to NM_000450.2 C516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr1:151337063 C>T maps to ENST00000435071 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr22:50654263 G>A maps to NM_031454.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr22:50649058 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:169586482 G>T maps to NM_003005.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr1:169564102 G>T maps to NM_003005.3 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:169580754 C>T maps to NM_003005.3 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:169563945 G>A maps to NM_003005.3 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:169578859 C>A maps to NM_003005.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:40006604 C>G maps to NM_182704.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr19:40006577 C>G maps to NM_182704.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:50310864 G>A maps to NM_004636.2 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:50313139 G>A maps to NM_004636.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:80418628 G>T maps to NM_006379.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:80387645 C>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr7:80378306 T>C maps to NM_006379.2 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr7:80439993 G>C maps to NM_006379.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:84644416 C>T maps to NM_152754.2 W554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:84702361 G>A maps to NM_152754.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr7:84649629 T>A maps to NM_152754.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:83037795 T>C maps to NM_012431.2 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr7:83014678 A>T maps to NM_012431.2 C602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:83029391 G>T maps to NM_012431.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr7:83119519 C>G maps to NM_012431.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:83014747 C>A maps to NM_012431.2 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr3:52476316 C>A maps to NM_020163.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr9:92006319 G>A maps to NM_006378.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr2:74881626 A>T maps to NM_004263.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:74901713 G>T maps to NM_004263.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:74906813 G>T maps to NM_004263.3 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:9190532 C>A maps to NM_003966.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:9227043 C>A maps to NM_003966.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:9237980 C>A maps to NM_003966.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr5:9202089 G>A maps to NM_003966.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:9154613 G>A maps to NM_003966.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr5:9202245 G>T maps to NM_003966.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr3:122645281 A>G maps to NM_001031702.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:122632821 G>T maps to NM_001031702.2 S672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr3:122634306 G>A maps to NM_001031702.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr3:122629800 G>A maps to NM_001031702.2 H1061H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:115824668 G>A maps to ENST00000257414 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr5:115782853 G>A maps to ENST00000257414 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:4552447 G>T maps to NM_032108.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:151108491 A>T maps to NM_001178061.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:151107753 G>A maps to NM_001178061.1 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr15:48062818 C>A maps to NM_153618.1 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:74704318 C>T maps to NM_003612.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr15:74704327 C>T maps to NM_003612.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr20:43836507 C>A maps to NM_003007.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr20:43836327 T>C maps to NM_003007.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr20:43836174 C>T maps to NM_003007.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr20:43850410 G>A maps to NM_003008.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr20:43851672 C>A maps to NM_003008.2 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr20:43850506 G>A maps to NM_003008.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:48457585 C>T maps to ENST00000004980 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr3:185337232 C>G maps to ENST00000427465 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:185316245 C>T maps to ENST00000427465 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr3:196613164 G>A maps to NM_152699.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:196626830 G>T maps to NM_152699.4 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr3:196654686 G>A maps to NM_152699.4 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:76388390 C>T maps to NM_015571.2 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:101062528 C>A did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:101086709 T>C maps to NM_020654.3 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:13361281 C>A maps to NM_012247.4 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr16:30456052 T>C maps to ENST00000478753 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:26142207 A>G maps to NM_020451.2 *591W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:26142089 G>T maps to NM_020451.2 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr4:25146714 A>T maps to NM_016955.3 L282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:30389811 C>T maps to NM_052838.3 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:110323373 G>C maps to ENST00000356688 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:55910745 G>T maps to NM_207366.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:55872949 C>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr2:242274554 G>T maps to ENST00000391972 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:42388702 C>T maps to NM_145733.2 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:118763347 G>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr17:75398372 G>T maps to NM_001113491.1 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:48283984 C>T maps to NM_003009.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr6:158538848 C>T maps to NM_032861.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:67895689 G>A maps to NM_001018067.1 P98P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-21-1077-01A-01D-1521-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:18029509 C>T maps to NM_012139.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:18014478 T>G maps to NM_012139.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr20:43129877 G>A maps to NM_006811.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr5:79442031 C>T maps to NM_001174072.1 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:150263868 G>A maps to NM_014445.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:94752573 C>T maps to NM_001100607.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr14:94752582 A>G maps to NM_001100607.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr14:94914712 G>C maps to NM_001080451.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr14:94964656 T>C maps to NM_173850.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr14:95081218 C>T maps to ENST00000393080 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr14:95033442 C>A maps to NM_006215.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:95030430 C>T maps to NM_006215.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:95029959 C>A maps to NM_006215.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:95054238 G>A maps to NM_000624.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr14:95053972 C>T maps to NM_000624.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr14:95054286 C>A maps to NM_000624.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:94772414 G>T maps to NM_001756.3 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:94780382 G>T maps to NM_001756.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr14:94780436 G>A maps to NM_001756.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:105280576 A>T did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:105279132 A>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:105279350 T>C did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:105280988 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:105280733 C>G did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr23:105280896 G>C did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:105279113 T>C did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr18:61600391 C>T maps to NM_005024.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:61233931 C>T maps to ENST00000382768 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr18:61228334 G>C maps to ENST00000382768 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr18:61231352 G>T maps to ENST00000382768 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr18:61226896 C>G maps to ENST00000382768 Y130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr18:61232706 G>C maps to ENST00000382768 T245T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-22-1012-01A-01D-1521-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr18:61256063 G>T maps to NM_012397.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr18:61570214 C>G maps to NM_001143818.1 Y308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr18:61328423 G>A maps to NM_006919.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr18:61305234 G>A maps to NM_002974.2 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr18:61304958 G>T maps to NM_002974.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr18:61306465 G>A maps to NM_002974.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr18:61306499 G>T maps to NM_002974.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr6:2954828 C>A maps to ENST00000316782 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:173883895 G>C maps to NM_000488.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:173878824 G>A maps to NM_000488.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:173880966 A>G maps to NM_000488.3 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:224866482 C>T maps to NM_001136530.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr11:57373645 C>T maps to ENST00000403558 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:167543033 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr3:167508223 G>T maps to NM_005025.4 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr3:167510552 G>A maps to NM_005025.4 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr3:167189517 T>C maps to NM_006217.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:167189508 G>T maps to NM_006217.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:64863519 G>C maps to NM_014755.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:30977241 C>T maps to NM_014712.1 F680F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr16:30991033 G>C maps to NM_014712.1 T1309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr3:47129613 C>A maps to NM_014159.6 E1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr14:99879359 G>A maps to NM_032233.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr1:150916461 C>T maps to NM_001145415.1 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:150900288 G>T maps to NM_001145415.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:135202916 G>C maps to ENST00000372169 P1356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:27291091 C>T maps to NM_178860.4 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:26706680 C>A maps to NM_021115.4 Y520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr22:26701972 C>T maps to NM_021115.4 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr22:26736443 C>T maps to NM_021115.4 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr22:26747015 A>C did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr16:29888688 G>A maps to NM_201575.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr16:29891242 G>T maps to NM_201575.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr16:29888631 T>A maps to NM_201575.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:64544042 C>T maps to NM_201995.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr22:30730594 C>T maps to NM_005877.4 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:38435241 C>G did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:38453318 C>A maps to NM_006802.2 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:198288680 G>A maps to NM_012433.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr11:65827323 C>G maps to NM_006842.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr16:70604042 G>A maps to NM_012426.4 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:70578409 C>T maps to NM_012426.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr1:149898739 T>C maps to NM_005850.3 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:19413071 A>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr22:32011204 G>A maps to NM_001007467.1 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr22:31946266 G>A maps to NM_001007467.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr10:7409782 C>T maps to NM_001018039.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr10:7409713 G>A maps to NM_001018039.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr10:7205845 A>T maps to NM_001018039.1 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr10:7218018 C>T maps to NM_001018039.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr1:27190281 G>A maps to NM_006142.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr8:41166483 C>A maps to NM_003012.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr7:37951815 T>C maps to ENST00000223214 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr10:99527576 C>T maps to NM_003015.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:70700377 G>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr1:70716349 A>G maps to NM_004768.3 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:19112430 G>T maps to NM_001017392.3 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr19:19135670 C>A maps to NM_001017392.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:19115331 C>A maps to NM_001017392.3 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr21:33044506 C>T maps to NM_020706.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr21:33067158 T>C maps to NM_020706.2 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr21:33074094 G>T maps to NM_020706.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:45567389 C>T maps to NM_007056.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:1712488 C>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:1720005 G>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:1714313 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:74733065 G>A maps to NM_003016.4 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr11:94800938 C>A maps to NM_032102.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr12:46321719 G>T maps to NM_004719.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:46321719 G>T maps to NM_004719.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr12:46320549 T>C maps to NM_004719.2 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr12:46320222 A>G maps to NM_004719.2 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:46321728 T>C maps to NM_004719.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:46316731 G>T maps to NM_004719.2 S1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:29475182 G>A maps to NM_005626.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr1:168208374 C>T maps to NM_199344.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr14:36946256 G>A maps to NM_001101341.1 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:81373496 C>T maps to NM_001093770.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:81373853 C>T maps to NM_001093770.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr10:104491931 C>A maps to NM_178858.4 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr10:102799339 T>C maps to NM_030971.3 *326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr4:52890290 G>C maps to NM_000232.4 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:156186334 G>A maps to NM_000337.5 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr5:156021963 T>C maps to NM_000337.5 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:156021940 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr13:23898646 C>T maps to NM_000231.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:14412336 C>T maps to NM_139167.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:14412435 C>T did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr8:13959959 G>T maps to NM_139167.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:153905614 A>G maps to NM_015595.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr1:67199523 C>A maps to ENST00000237247 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:67142742 G>T maps to ENST00000237247 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:67205145 C>A maps to ENST00000237247 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:67185067 C>T maps to ENST00000237247 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:67109380 C>A maps to ENST00000237247 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr6:134495879 T>G maps to NM_005627.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr6:134495936 C>T maps to NM_005627.3 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr15:77471835 C>T maps to NM_024776.2 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr15:77473982 C>A maps to NM_024776.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr15:77472962 C>A maps to NM_024776.2 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:77450848 G>A maps to NM_024776.2 N1109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr15:77407451 C>T maps to NM_024776.2 T1429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr15:77425757 C>T maps to NM_024776.2 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr15:77425618 G>A maps to NM_024776.2 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:67726103 A>G maps to NM_013257.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr8:67755685 G>C did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr4:108816945 G>A maps to NM_152621.5 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr3:20212599 T>A maps to NM_001012410.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr3:20225132 T>C maps to NM_001012410.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:201436175 T>C maps to NM_152524.5 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:201436385 G>T maps to NM_152524.5 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:72614557 C>T maps to NM_003901.3 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:64165360 C>A maps to NM_030791.2 G234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr2:223386572 C>T maps to NM_152386.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:78184601 G>T maps to NM_000199.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:25264493 C>T maps to NM_001039948.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:2279102 G>A maps to NM_014853.2 E806E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr17:2266299 G>T maps to NM_014853.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:40802121 C>T maps to NM_015705.4 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:123504097 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:123499664 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:6760857 C>T maps to NM_005490.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr19:6752604 C>T maps to NM_005490.2 *577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:21051068 G>A maps to ENST00000444387 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:85663659 C>T maps to NM_198482.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:80532629 C>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr22:38039102 A>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:235950605 C>G maps to NM_014521.2 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:249106515 C>A maps to NM_030645.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:249106335 C>A maps to NM_030645.1 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:152054353 C>A maps to NM_001009555.3 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:4366963 C>A maps to NM_003025.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:87207946 C>G maps to ENST00000482504 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:87208107 C>T maps to ENST00000482504 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:19713855 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:19764485 C>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:19568201 C>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:19564055 G>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:105361812 G>A maps to ENST00000369774 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr10:105372886 C>A maps to ENST00000369774 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:171766401 G>A maps to NM_001017995.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr5:171766539 A>T maps to NM_001017995.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr4:170057543 G>A maps to NM_020870.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:145383660 G>A maps to NM_152550.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr5:145439471 C>T maps to NM_152550.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:8229800 C>T maps to NM_018986.3 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:8226900 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:8229026 G>T maps to NM_018986.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr4:8229142 C>G maps to NM_018986.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:148427423 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:51165683 C>T maps to ENST00000391814 E2016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:51200904 C>T maps to ENST00000391814 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr11:70332959 C>A maps to ENST00000338508 P1140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:70332941 C>T maps to ENST00000338508 E1146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:70332824 C>A maps to ENST00000338508 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:70333106 C>T maps to ENST00000338508 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:70333550 C>G maps to ENST00000338508 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr11:70333106 C>T maps to ENST00000338508 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:51117846 C>G maps to NM_001080420.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr22:51117756 C>T maps to NM_001080420.1 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:425193 C>A maps to NM_012435.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr19:425172 C>T maps to NM_012435.2 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:91653063 G>C maps to NM_016848.5 Y500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr15:49254906 C>T maps to NM_203349.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr15:45491043 T>A maps to ENST00000437903 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:155598996 C>T maps to NM_000193.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr13:26621139 G>T maps to NM_001007538.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr4:42403074 G>T maps to NM_001080505.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:201859587 G>A maps to NM_198149.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:41097082 C>T maps to NM_138392.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:41083300 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:18257059 G>A maps to NM_004169.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:18250932 C>A maps to NM_004169.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr12:57626300 C>G maps to NM_005412.5 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:601813 T>C did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:601562 T>A did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:591827 T>A did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:601572 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:591647 G>C did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:157820670 G>A maps to NM_003030.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:146262958 C>A maps to ENST00000367503 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:146244843 C>T maps to ENST00000367503 Q1169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:72891500 C>A maps to NM_018130.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:132158541 C>A maps to NM_001172700.1 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:9864570 G>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:9862558 G>C did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:9864197 C>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:9905278 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:9905623 G>C did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:9863736 C>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr4:77661305 A>G maps to NM_020859.3 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr4:77662002 C>T maps to NM_020859.3 Q893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:77661233 C>G maps to NM_020859.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr4:77662652 C>A maps to NM_020859.3 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr4:77662455 A>T maps to NM_020859.3 R1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr23:50377040 T>C did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:50376729 G>T did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr23:50341343 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:50350934 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:50351167 T>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:50350965 G>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:50377426 C>G did not map to a codon.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr23:50341477 C>G did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:164793778 C>A maps to NM_001041.3 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:164700132 G>T maps to NM_001041.3 S1771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:164700155 T>A maps to NM_001041.3 K1764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr3:164716461 C>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:164754252 A>T maps to NM_001041.3 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:164755795 C>T maps to NM_001041.3 W773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:164766994 G>T maps to NM_001041.3 C545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:124508524 C>T maps to NM_170601.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr3:113329992 T>C did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:113329853 G>C did not map to a codon.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:113327363 T>C maps to ENST00000393830 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:113320480 C>T maps to ENST00000393830 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr11:117062729 G>C maps to NM_001040455.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:117063910 C>A maps to NM_001040455.1 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr11:117066727 G>C maps to NM_001040455.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr20:3670648 G>C maps to NM_023068.3 V1618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr20:3670822 C>T maps to NM_023068.3 P1560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:50463851 C>G maps to NM_052884.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:50462098 G>A maps to NM_052884.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr19:52004681 C>T maps to NM_053003.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:52003231 C>A maps to ENST00000441969 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr19:52001374 A>T maps to NM_053003.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:52004756 G>T maps to NM_053003.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr19:52004672 G>A maps to NM_053003.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:52148736 T>A maps to NM_001098612.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:52147257 C>A maps to NM_001098612.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:52147191 C>A maps to NM_001098612.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:52147134 G>T maps to NM_001098612.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr19:52148781 A>G maps to NM_001098612.1 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:52034753 C>G maps to NM_001245.5 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:52023371 G>T maps to NM_001245.5 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr19:52034460 C>T maps to NM_001245.5 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:52033941 A>G maps to NM_001245.5 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:51645694 G>A maps to NM_014385.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr19:51650534 C>A maps to NM_014385.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:51647759 G>T maps to NM_014385.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr19:51647819 C>A maps to NM_014385.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr19:51958759 C>T maps to NM_014442.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:51628377 C>A maps to NM_014441.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr19:51628947 G>A maps to NM_014441.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:116729285 G>A maps to ENST00000445177 T958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:116719897 C>A maps to ENST00000445177 E1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr11:116732020 G>C maps to ENST00000445177 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr5:138356903 G>T maps to ENST00000509534 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr12:56355203 C>T maps to NM_006928.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:100838802 C>A maps to ENST00000262901 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:100895256 G>T maps to ENST00000262901 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr6:100896434 G>T maps to ENST00000262901 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr6:100841639 G>A maps to ENST00000262901 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:100838338 G>T maps to ENST00000262901 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:100838800 C>T maps to ENST00000262901 E579E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:100838428 C>T maps to ENST00000262901 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr6:100838773 G>T maps to ENST00000262901 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:75676636 C>A maps to NM_001145357.1 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr14:72138261 C>T maps to NM_015556.1 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr14:72085579 C>T maps to NM_015556.1 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:72205014 G>A maps to NM_015556.1 L1748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr14:72190543 G>C maps to NM_015556.1 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr14:72138133 G>T maps to NM_015556.1 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:232574960 G>A maps to NM_020808.3 D1308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:232619558 G>A maps to NM_020808.3 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr1:232650419 G>A maps to NM_020808.3 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:232551264 G>C maps to NM_020808.3 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:232579346 C>A did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr1:232649735 G>A maps to NM_020808.3 C450C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:232600906 C>A maps to NM_020808.3 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:38591795 C>T maps to NM_015073.1 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:38610203 C>G maps to NM_015073.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr19:38689101 G>A maps to NM_015073.1 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:1915373 G>T maps to ENST00000400068 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr20:1552434 C>A maps to NM_006065.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:218843 C>A maps to NM_012239.5 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:13592055 C>T maps to NM_012241.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr19:4174903 C>A maps to NM_016539.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr9:35650381 C>T maps to NM_014450.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:61113135 G>A maps to NM_005982.3 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr14:61115902 G>T maps to NM_005982.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:45233548 C>A maps to NM_016932.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr14:61190687 C>A maps to NM_017420.4 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:46269049 G>A maps to NM_175875.4 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr18:47906587 C>T maps to NM_145060.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:2160702 C>A maps to NM_003036.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:170078994 G>T maps to NM_005414.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr6:31937151 G>A maps to NM_006929.4 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr6:31936518 C>T maps to NM_006929.4 F1042F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:31936486 C>T maps to NM_006929.4 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr8:134062193 A>C maps to NM_006748.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr20:35242817 G>T maps to NM_032214.2 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr13:78334966 A>T maps to ENST00000389459 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:160607206 G>T maps to NM_003037.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr1:160607106 T>A maps to NM_003037.2 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:160465905 G>T maps to NM_001184714.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr1:160465887 G>T maps to NM_001184714.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:159799839 C>T maps to NM_020125.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr14:70245070 C>A maps to NM_003049.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr13:103718329 A>G maps to NM_000452.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr13:103718500 G>T maps to NM_000452.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:153716115 C>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr8:82606862 A>T maps to NM_001010893.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:82606631 C>T maps to NM_001010893.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr12:51402303 G>A maps to NM_001174125.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr12:51386098 T>C maps to NM_001174125.1 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:48577446 G>A did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr15:48561892 G>T maps to NM_000338.2 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr15:48594976 A>T maps to NM_000338.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr15:48548077 C>A maps to NM_000338.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr5:127520117 A>G maps to NM_001046.2 Q1120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:127420338 C>A maps to NM_001046.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr16:56936404 G>A maps to NM_000339.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr16:56913033 C>T maps to NM_000339.2 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr16:56928500 G>A maps to NM_000339.2 K869K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:56917982 C>T maps to NM_000339.2 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr16:56947292 C>T maps to NM_000339.2 N1023N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:67980941 G>C maps to NM_005072.4 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr20:44663629 C>G maps to NM_001134771.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:44664528 G>A maps to NM_001134771.1 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr20:44685077 G>A maps to NM_001134771.1 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr20:44666021 C>T maps to NM_001134771.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:44665999 C>A maps to NM_001134771.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr20:44663662 G>A maps to NM_001134771.1 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr20:44664041 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:1087029 G>A maps to NM_006598.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:124802766 G>A maps to NM_001195483.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:100452290 G>T maps to NM_020246.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr7:100459151 G>T maps to NM_020246.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:100451836 A>T maps to NM_020246.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:100459085 C>G maps to NM_020246.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr7:122755643 C>T maps to NM_022444.3 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr7:122755607 C>A maps to NM_022444.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr20:45228638 C>T maps to NM_022829.5 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr20:45192145 G>C maps to NM_022829.5 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:135387594 C>A maps to NM_012450.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr7:135378966 G>A maps to NM_012450.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr18:43316431 C>A maps to NM_001146037.1 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr18:43329864 C>T maps to NM_001146037.1 N429N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr18:43217029 T>C maps to NM_007163.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr18:43204691 C>T maps to NM_007163.3 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr18:43243837 C>T maps to NM_007163.3 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:43207094 C>A maps to NM_007163.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:60714116 G>C maps to NM_016582.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr12:129294640 G>C maps to ENST00000376744 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr12:129299344 G>A maps to ENST00000376744 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:129299465 G>T maps to ENST00000376744 C232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr10:91198521 G>C maps to NM_213606.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:73744337 C>A did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:73740855 C>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:73096606 C>T maps to ENST00000450736 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:66267058 G>T maps to NM_004694.4 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr17:66267715 G>T maps to NM_004694.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:60168609 C>T maps to NM_004731.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr12:60169074 G>C maps to NM_004731.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr12:60169161 C>T maps to NM_004731.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr6:25826861 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:25811930 G>C maps to NM_005074.3 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:25811765 G>C maps to NM_005074.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:25850058 A>T maps to NM_001098486.1 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:25769300 C>G maps to NM_005495.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:25773530 C>T maps to NM_005495.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr6:25771235 C>A maps to NM_005495.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr6:74331541 C>T maps to NM_012434.4 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr6:74304841 T>C maps to NM_012434.4 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:22363310 C>G maps to NM_020346.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr11:22363154 G>A maps to NM_020346.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:22399220 G>T maps to NM_020346.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:22399181 C>T maps to NM_020346.2 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr11:22364890 G>T maps to NM_020346.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:22399018 T>A maps to NM_020346.2 Y494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:49939820 G>A maps to NM_020309.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr19:49937934 G>C maps to NM_020309.3 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:100774479 A>T maps to NM_139319.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:100796215 G>T maps to NM_139319.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr8:20007192 C>T maps to NM_001135691.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:119012936 G>C maps to NM_003054.4 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:119003707 C>T maps to NM_003054.4 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr10:119013586 C>T maps to NM_003054.4 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr10:50819811 C>G maps to NM_003055.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr11:35313934 G>A maps to NM_004171.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr5:36608602 A>G maps to NM_004172.4 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:47285695 G>T maps to NM_005628.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr19:15061012 A>T maps to NM_005071.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:53569102 C>A maps to NM_006671.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr1:53555551 G>T maps to NM_006671.4 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:53569153 G>C maps to NM_006671.4 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:53554563 C>A maps to NM_006671.4 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:53555557 G>C maps to NM_006671.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr8:42294927 C>A maps to NM_006749.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr6:160553334 C>A maps to NM_003057.2 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr6:160553344 C>G maps to NM_003057.2 Y199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr6:160557643 G>A maps to NM_003057.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr11:63059061 A>T maps to NM_001039752.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr11:63071613 G>T maps to NM_001039752.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:64326617 G>A maps to NM_018484.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:38318954 G>C maps to NM_004256.3 *552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr6:110746251 A>G maps to NM_033125.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr6:110746144 G>A maps to NM_033125.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:23816672 G>A maps to NM_020372.2 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:23817724 G>A maps to NM_020372.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr11:2946384 C>G maps to NM_002555.5 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr6:160679417 G>A maps to NM_003058.3 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:160671685 T>A maps to NM_003058.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr5:131630482 G>C maps to NM_003059.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr11:62747413 G>T maps to NM_004790.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr11:62749402 G>A maps to NM_004790.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr20:19677555 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr20:19665874 A>T maps to NM_020689.3 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:92908487 C>A maps to NM_153646.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr14:92900299 C>T maps to NM_153646.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:92949174 C>A maps to NM_153646.3 Y469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:48426491 C>T maps to NM_205850.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr15:48426536 A>G maps to NM_205850.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr15:48434508 A>T maps to NM_205850.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr12:113758148 C>A maps to NM_024959.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:79686895 C>G maps to ENST00000331531 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:4843193 C>A maps to NM_003562.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:172700881 G>T maps to NM_003705.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:95750513 C>A maps to NM_001160210.1 G674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:95751057 C>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr22:41173354 G>A maps to NM_006358.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr22:41195075 T>A maps to NM_006358.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:48895966 C>T maps to NM_000387.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr14:37180663 T>A maps to NM_030631.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:6454033 G>A maps to NM_024103.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:108700227 C>A maps to NM_013386.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr9:130869707 C>A maps to ENST00000373069 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr10:101370857 T>C maps to NM_031212.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr13:45980020 C>A maps to NM_001010875.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr4:128651828 G>C maps to NM_031291.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:9642480 C>T maps to NM_032315.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr1:9613681 A>C did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr8:23428852 A>T maps to NM_016612.2 K168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr17:42398094 C>G maps to NM_001143780.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr4:186066997 C>A maps to NM_001151.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr7:87477195 T>A maps to NM_018843.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:87483530 G>A maps to NM_018843.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:118544309 G>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:65147352 A>G maps to NM_182556.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:118604024 G>C did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:1505503 C>G did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr7:107430024 T>A maps to NM_000111.2 K227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr7:107342502 G>A did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr7:107341589 G>A maps to NM_000441.1 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:107323901 G>C maps to NM_000441.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr7:107353039 G>T maps to NM_000441.1 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:107329635 T>C maps to NM_000441.1 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:103014875 G>C maps to ENST00000354356 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:48665950 G>A maps to NM_022911.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr3:48670976 C>A maps to NM_022911.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr8:92307880 C>T maps to NM_134266.1 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:92406200 A>G maps to NM_134266.1 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:92378878 T>A maps to NM_134266.1 Y520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:92352655 G>C maps to NM_134266.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr6:35949980 C>G did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:205896718 G>A maps to NM_134325.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr19:17581501 G>C maps to NM_198580.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr1:153751661 G>C maps to ENST00000271857 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr9:131110860 C>T maps to NM_005094.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr19:59012685 G>A maps to NM_012254.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr5:128301898 G>C maps to NM_001017372.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:128302172 G>T maps to NM_001017372.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr5:128320940 C>A maps to NM_001017372.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr15:85438312 C>T maps to NM_004213.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr15:85438319 C>T maps to NM_004213.3 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr15:85438169 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr15:85478749 G>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr15:45556869 G>A maps to NM_004212.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:45564583 T>A maps to NM_004212.3 C580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr15:45556902 G>C maps to NM_004212.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr9:86900905 G>C maps to NM_022127.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr6:44199198 G>C did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr6:44197763 C>A maps to ENST00000313248 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr7:5338674 C>T maps to NM_153247.2 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:43395311 G>C maps to NM_006516.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:43392785 G>A maps to NM_006516.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr22:24224727 C>T maps to NM_030807.3 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr22:24210775 G>T maps to NM_030807.3 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:134350674 G>T maps to NM_145176.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr6:134349792 C>A maps to NM_145176.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr12:40265600 T>C maps to NM_052885.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr12:40422283 C>G maps to NM_052885.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:40441917 T>C maps to NM_052885.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:7984255 G>A maps to NM_153449.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr12:7985368 G>T maps to NM_153449.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:7980132 G>T maps to NM_153449.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:7982359 A>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:7984327 C>T maps to NM_153449.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr3:170744447 A>G maps to NM_000340.1 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:8074149 G>A maps to NM_006931.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:9118276 C>G maps to NM_003039.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr9:136338229 C>A maps to NM_017585.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:9075205 G>A maps to NM_207420.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr1:9083026 G>A maps to NM_207420.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:9998457 G>A maps to NM_020041.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:220091806 G>A maps to NM_018713.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:26369941 A>G maps to NM_001004434.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:26371486 C>G did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:27480120 G>T maps to NM_003459.4 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr15:45814459 G>A maps to NM_013309.4 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr5:68419158 C>A maps to NM_022902.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:32445320 G>T maps to NM_001193513.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:101377732 G>T maps to NM_133496.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr8:118170056 C>A maps to NM_173851.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr8:118184796 G>A maps to NM_173851.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr8:118173998 A>T maps to NM_173851.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr8:118184796 G>A maps to NM_173851.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr9:115925106 A>G maps to ENST00000394724 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr20:37356471 C>T maps to NM_080552.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr20:37353630 C>A maps to NM_080552.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr3:155571666 C>T maps to NM_004733.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:140126165 C>T maps to NM_080877.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr6:88221169 G>T maps to NM_006416.4 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:48762629 G>C did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:48767183 G>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr3:112300034 G>T maps to NM_017945.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr11:45832693 G>T maps to NM_018389.4 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:67515496 A>G maps to NM_015139.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr1:67518531 G>T maps to NM_015139.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr9:99114387 T>A maps to NM_007001.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:137245752 C>A maps to NM_001008783.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr6:137245644 C>T maps to NM_001008783.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:16664517 G>T maps to NM_024881.4 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr1:1666130 G>A maps to NM_182838.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:118556696 A>G maps to NM_001029858.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr6:118635204 T>A maps to NM_001029858.3 Y339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr1:234367238 G>A maps to NM_173508.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:234445021 T>C maps to NM_173508.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:234458778 C>A maps to NM_173508.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr2:114512813 C>T maps to NM_025181.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr2:114483082 T>C maps to NM_025181.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:150856201 C>T maps to NM_078483.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:150856314 C>A maps to NM_078483.2 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:150701634 G>A maps to NM_181776.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:150726877 C>T maps to NM_181776.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr11:92881959 C>A maps to NM_152313.2 G420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:92895909 G>A maps to NM_152313.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:124947394 C>T maps to NM_198277.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:79263497 G>A maps to NM_001037984.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:79250893 T>A maps to NM_001037984.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:79219574 G>A maps to NM_001037984.1 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr17:79226319 C>T maps to NM_001037984.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:47178370 C>A maps to NM_018018.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:48317371 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:48317958 G>T did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:48318222 C>G did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr16:58706124 A>G maps to NM_018231.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr16:84050256 C>A maps to NM_001080442.1 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:84075714 G>A maps to NM_001080442.1 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:54929712 G>A maps to NM_173514.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:196578164 G>A maps to NM_001127257.1 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:196548475 C>T maps to NM_001127257.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:196599665 G>T maps to NM_001127257.1 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr17:71027693 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr10:18250592 T>A maps to NM_001145195.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:18292098 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:18242258 C>A maps to NM_001145195.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:2733003 G>A maps to NM_144564.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr8:145638175 G>A maps to NM_130849.2 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr12:56628612 G>C maps to NM_001135195.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr18:33706700 G>T maps to NM_012319.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:44547705 C>T maps to NM_000341.3 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr11:62653040 G>A maps to NM_001012661.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:62655846 G>A maps to NM_001012661.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:190430287 G>A maps to NM_014585.5 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr2:190437667 C>A maps to NM_014585.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr12:105282955 C>A did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr11:57268683 G>C maps to NM_003627.5 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr11:57176680 G>T maps to ENST00000428603 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr9:108128710 G>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr19:10745907 C>T maps to NM_020428.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:31833699 G>C maps to NM_025257.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr6:31833153 G>A maps to NM_025257.2 Y566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr1:75693534 C>T maps to NM_152697.4 W287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:75699736 G>A maps to NM_152697.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:8398049 C>G maps to ENST00000377479 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:205632639 G>A maps to NM_033102.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:205632420 G>A maps to NM_033102.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:142222526 C>T maps to NM_001080431.1 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:142238344 G>A maps to NM_001080431.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr8:142228415 C>G maps to NM_001080431.1 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:19452968 G>A maps to ENST00000395585 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr17:42332031 T>C did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:162661103 T>C maps to NM_001178015.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:162719516 T>C maps to NM_001178015.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:162762166 A>C maps to NM_001178015.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:162833287 C>A maps to NM_001178015.1 I1082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:162804143 T>C maps to NM_001178015.1 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr2:162760660 G>T maps to NM_001178015.1 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:3218265 A>G maps to NM_032034.3 H20H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr20:3211588 G>A maps to NM_001174090.1 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr20:3218259 A>G maps to NM_032034.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:27900641 G>A maps to NM_018158.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:27887972 G>T maps to NM_018158.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:27890250 C>T maps to NM_018158.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:150771337 C>T maps to NM_003040.3 F916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr7:150761613 C>A maps to NM_003040.3 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr7:150773152 C>T maps to NM_003040.3 A1175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:220501123 G>T maps to NM_201574.2 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:220504423 C>A maps to NM_201574.2 R1109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:220501520 G>A maps to NM_201574.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr4:72121046 G>T maps to NM_001098484.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr4:72316225 G>T maps to NM_001098484.2 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr4:72263357 G>C maps to NM_001098484.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr4:72412221 A>G maps to NM_001098484.2 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr4:72222839 G>T maps to NM_001098484.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:27439273 G>T maps to ENST00000454389 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr22:32477932 A>G maps to NM_000343.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr22:32506091 G>A maps to NM_000343.3 K629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr22:32487723 G>T maps to NM_000343.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr17:18862954 G>C maps to NM_152351.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr16:24921721 C>T maps to NM_052944.2 N582N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr16:24902388 G>A maps to NM_052944.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr16:24895426 A>T maps to NM_052944.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr16:24920377 C>A maps to NM_052944.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr16:24918056 C>A maps to NM_052944.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:26718756 C>A maps to NM_178498.3 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr16:31494561 G>A maps to ENST00000431354 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr22:32625227 G>A maps to NM_014227.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:17985515 T>C maps to NM_000453.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:17986876 C>G maps to NM_000453.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:17983412 T>A maps to NM_000453.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:27426648 G>C maps to NM_021095.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:27429762 C>G maps to NM_021095.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:27424658 C>A maps to NM_021095.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr2:108609582 G>T maps to NM_021815.2 G150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:108608571 C>T maps to NM_021815.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr2:108608586 C>T maps to NM_021815.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:101603488 C>T maps to NM_145913.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr12:101603401 G>T maps to NM_145913.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr12:101576587 T>C maps to NM_145913.3 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:101603341 C>T maps to NM_145913.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:48703479 C>T maps to NM_001135181.1 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:48713067 G>A maps to NM_001135181.1 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:332340 C>A maps to NM_016615.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:344276 G>C maps to NM_016615.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:330113 C>T maps to NM_016615.3 *603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr12:330115 A>G maps to NM_016615.3 *603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:115577986 A>C did not map to a codon.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr23:115574931 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:115577906 G>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:115582713 T>A did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:49797731 G>T maps to NM_014037.2 Y436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr19:49813645 G>A maps to NM_014037.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:49814439 C>T maps to NM_014037.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:110717572 C>T maps to NM_001010898.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr5:1232343 C>T maps to NM_182632.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr5:1238096 G>T maps to NM_182632.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr5:1213603 C>G maps to NM_001003841.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr5:1219620 C>T maps to NM_001003841.2 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr16:55719105 G>T maps to NM_001043.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:55719165 C>G maps to NM_001043.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:55731807 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:1422014 C>T maps to NM_001044.4 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr5:1422080 C>G maps to NM_001044.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr5:1416274 G>T maps to NM_001044.4 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr5:1432760 G>A maps to NM_001044.4 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr5:1420683 A>G maps to NM_001044.4 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr5:1432616 G>A maps to NM_001044.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:28543168 G>T maps to ENST00000394821 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr11:20657898 G>T maps to NM_004211.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr11:20625905 G>T maps to NM_004211.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:20660003 G>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:20636264 G>A maps to NM_004211.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:152959700 C>G did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:152959802 G>T did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr13:30091887 G>C maps to NM_003045.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr13:30096467 G>T maps to NM_003045.4 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr13:30104820 C>A maps to NM_003045.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:33703208 A>T maps to NM_019849.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:87235207 G>T maps to NM_138817.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:87242188 C>A maps to NM_138817.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr8:87226773 C>G maps to NM_138817.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:170198774 T>C maps to NM_020949.2 Q432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:170198249 C>T maps to NM_020949.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:70148089 G>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:70145714 C>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:70148756 C>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:87874693 C>G maps to NM_003486.5 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr14:23242899 G>T maps to NM_001126106.1 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr14:23607194 G>A maps to NM_012244.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:33350755 C>G maps to NM_014270.4 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:33349398 A>G maps to NM_014270.4 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:33355640 G>A maps to NM_014270.4 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr2:40656931 T>C maps to NM_021097.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr2:40387974 T>C maps to NM_021097.2 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr2:40656126 T>A maps to NM_021097.2 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:40656772 G>T maps to NM_021097.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr2:40656651 G>A maps to NM_021097.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:40405578 G>A maps to NM_021097.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr2:40656544 G>A maps to NM_021097.2 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:47951364 G>A maps to NM_015063.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:70515754 C>T maps to NM_183002.1 G712G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-22-4613-01A-01D-1441-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:70522528 C>A maps to NM_183002.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr14:70634926 C>A maps to NM_183002.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:111918266 C>T maps to NM_183061.1 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr3:111927156 G>A maps to NM_183061.1 Y618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:111999532 T>C maps to NM_183061.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:173526508 G>T maps to NM_178527.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:173569254 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:173478802 G>C maps to NM_178527.3 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr5:485313 C>G maps to NM_004174.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:482233 C>A maps to NM_004174.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr5:484768 C>A maps to NM_004174.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:103142716 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:103095402 C>A maps to NM_001011552.3 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:103125361 A>G maps to NM_001011552.3 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr16:67286511 G>A maps to NM_004594.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr16:67289689 C>T maps to NM_004594.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:135080639 G>A did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:135067758 C>T did not map to a codon.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr23:46502716 T>C did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:46510818 A>G did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr20:48491341 C>A maps to ENST00000417961 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:143412109 A>G maps to NM_173653.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:143297492 C>A maps to NM_173653.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr3:143551031 A>G maps to NM_173653.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr3:142985588 A>T maps to NM_173653.3 Y631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:142985729 C>T maps to NM_173653.3 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:21453299 T>A maps to NM_134431.3 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr12:21422582 C>A maps to NM_134431.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr12:21453280 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr12:21450347 G>T maps to NM_134431.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:21331905 G>T maps to NM_006446.4 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr12:21392003 G>T maps to NM_006446.4 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:21377755 T>C maps to NM_006446.4 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr12:21349928 G>A maps to NM_006446.4 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr12:21327634 C>T maps to NM_006446.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:21028280 G>A maps to NM_019844.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr12:21011371 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:21008008 T>A maps to NM_019844.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr12:21028331 T>C maps to NM_019844.2 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr12:21032523 C>T maps to NM_019844.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr12:21015493 T>A did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr12:20858881 G>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr12:20876024 T>C maps to NM_017435.4 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr12:20893185 A>G maps to NM_017435.4 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:133692603 C>A maps to NM_005630.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr3:133670153 C>T maps to NM_005630.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr3:133666116 G>T maps to NM_005630.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr3:133692621 C>A maps to NM_005630.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:74913990 C>T maps to NM_007256.4 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:74880410 C>A maps to NM_007256.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr11:74883490 T>A maps to NM_007256.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr5:101627152 C>T maps to NM_180991.4 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr5:101583091 C>A maps to NM_180991.4 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr8:70585234 C>A maps to NM_030958.2 E806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr8:70744098 C>G maps to NM_030958.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr8:70617408 T>G maps to NM_030958.2 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:70744041 T>C maps to NM_030958.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:101735365 C>T maps to NM_173488.3 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:101834338 G>A maps to NM_173488.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr5:101755708 T>A maps to NM_173488.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr5:101816025 C>A maps to NM_173488.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr5:101735266 G>T maps to NM_173488.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr17:33690214 G>A maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr17:33689941 G>A maps to NM_152270.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr17:33749255 G>A maps to NM_018042.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:33738499 T>A maps to NM_018042.3 K532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:33592327 C>T maps to NM_144975.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:98766299 C>T maps to NM_003061.2 R1173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:98761030 G>A maps to NM_003061.2 R1481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:98819233 G>A maps to NM_003061.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr4:20598113 G>T maps to ENST00000273739 G1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:20525490 G>A maps to ENST00000273739 K417K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:20619196 G>A maps to ENST00000273739 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:20525427 T>C maps to ENST00000273739 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr4:20598064 C>G maps to ENST00000273739 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr4:20598037 T>C maps to ENST00000273739 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:20620526 G>T maps to ENST00000273739 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr4:20611672 G>T maps to ENST00000273739 E1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr5:168093539 G>A maps to NM_003062.2 Y1497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:168199839 G>A maps to NM_003062.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:168216563 C>A did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr5:168199834 G>T maps to NM_003062.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:168216617 C>T maps to NM_003062.2 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr13:84454187 G>A maps to NM_052910.1 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:84454901 C>A maps to NM_052910.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr13:84455288 G>A maps to NM_052910.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr13:84455096 G>C maps to NM_052910.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr13:84454196 C>A maps to NM_052910.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr13:84455474 C>T maps to NM_052910.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:144904755 C>T did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:144905218 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:144905920 T>A did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:144905393 G>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:144904015 G>C did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:144905785 G>C did not map to a codon.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr23:144904177 C>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:144904037 G>C did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:144906361 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:164906910 G>A maps to NM_014926.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:164906743 G>T maps to NM_014926.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:164908291 C>T maps to NM_014926.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr3:164907778 G>A maps to NM_014926.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:164905963 T>C maps to NM_014926.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:164907139 C>T maps to NM_014926.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:164906518 G>A maps to NM_014926.2 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr3:164907319 G>A maps to NM_014926.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr3:164905717 G>T maps to NM_014926.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:164907646 G>A maps to NM_014926.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr3:164905810 G>T maps to NM_014926.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr3:164905717 G>C maps to NM_014926.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:142717781 C>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:142716936 G>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:142718579 G>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:142717524 C>A did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:142718644 T>A did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr23:142716935 G>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:142717086 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:142718107 G>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:142718089 G>A did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr13:88327855 C>A maps to NM_015567.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr13:88329601 C>G maps to NM_015567.1 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr13:88329934 C>T maps to NM_015567.1 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr13:86369449 A>G maps to NM_032229.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr13:86368470 C>A maps to NM_032229.2 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr10:105779490 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:57611615 T>A maps to NM_016045.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr15:59191708 C>T maps to NM_024755.2 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr15:59225620 G>C maps to NM_024755.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr5:159839519 G>A maps to NM_006425.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr8:143823220 C>A maps to NM_020427.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:146479016 C>T maps to NM_001003688.1 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:146436165 G>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:67358512 C>T maps to NM_005902.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr15:67457286 C>A maps to NM_005902.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr18:48604809 G>T maps to NM_005359.5 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr18:48604753 G>T maps to NM_005359.5 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr18:48584786 C>T maps to NM_005359.5 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr18:48581242 C>T maps to NM_005359.5 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr18:46476229 C>A maps to NM_005904.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:71567877 C>T maps to NM_001044305.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:40879886 G>A maps to NM_022733.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:128645951 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:128657244 G>C did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:128623053 T>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:128630822 C>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr23:128650318 A>C did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:128649953 G>A did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr23:128599710 T>G did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:128649886 A>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr9:2116021 C>T maps to NM_003070.3 A1219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:2033004 C>A maps to NM_003070.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr19:11114046 G>T maps to NM_001128849.1 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr19:11096081 G>T did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr4:144457611 C>A maps to NM_003601.2 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr4:144468619 A>G maps to NM_003601.2 Q912Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:47742766 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:56575864 T>A did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr12:56572239 G>A maps to NM_003075.3 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr12:56563644 G>C maps to NM_003075.3 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr12:56568478 G>A maps to NM_003075.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:150939641 C>A maps to NM_003078.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr17:38788533 C>T maps to NM_003079.4 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:53439104 G>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:53439032 G>A did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:53440301 C>T did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr22:45802339 C>A did not map to a codon.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr22:45802743 C>A maps to NM_148674.3 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr22:45779396 C>A maps to NM_148674.3 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:106891964 G>T maps to NM_001042550.1 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr10:112359486 G>T maps to NM_005445.3 G782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr10:112344087 T>C maps to NM_005445.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:160150073 G>T maps to NM_005496.3 E1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:72962527 G>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:18167820 C>T maps to NM_148886.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr22:39908483 C>G maps to NM_019008.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr22:39908031 G>A did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr22:39908336 T>G maps to NM_019008.4 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:18221364 C>T maps to NM_144775.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:55786012 A>G maps to NM_001122964.1 N784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:18844346 G>A maps to ENST00000389467 L2903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:18887444 C>A did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr16:18870956 G>A maps to ENST00000389467 Q1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:18840912 G>A maps to ENST00000389467 Q3100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr16:18830964 A>G maps to ENST00000389467 A3252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr16:18827848 G>A maps to ENST00000389467 D3360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:18893615 G>A maps to ENST00000389467 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:156244451 T>A maps to NM_015327.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr17:2202477 C>T maps to NM_017575.4 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr1:183495813 A>G maps to ENST00000367537 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:70444655 T>A maps to NM_001034852.1 L167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr16:68404962 C>T maps to NM_018667.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr4:71232479 T>C maps to NM_012390.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr4:71227858 C>A maps to NM_012390.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr4:71232554 C>G maps to NM_012390.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:21990681 G>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:21995301 A>T did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr9:33053168 C>A maps to NM_018225.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:98645443 C>A maps to NM_020429.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:214454740 G>T maps to NM_020197.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:246498752 C>T maps to NM_001167740.1 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:246078936 G>T maps to NM_001167740.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:1687710 G>A maps to NM_052928.2 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:73453005 G>T maps to NM_006062.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr8:49832866 A>G maps to NM_003068.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr8:49832653 C>T maps to NM_003068.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr20:10280020 C>T maps to NM_130811.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr22:21224806 C>A maps to NM_004782.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:227947171 C>G maps to NM_053052.3 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:84368747 C>T maps to NM_014841.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:84290220 G>T maps to NM_014841.2 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr6:84417640 C>A maps to NM_014841.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:84290167 C>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr9:139288771 C>T maps to NM_003086.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:153631257 G>T maps to NM_012437.4 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:176047817 C>T maps to NM_003085.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:176048304 C>T did not map to a codon.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr7:127544838 A>G maps to NM_014390.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr7:127727087 C>T maps to NM_014390.2 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:127338938 G>T maps to NM_014390.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:38003386 C>A maps to NM_024700.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:38005789 A>T maps to NM_024700.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:1277020 C>T maps to ENST00000381876 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr20:1277857 T>A maps to ENST00000381876 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr2:96969004 C>A maps to NM_014014.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:96950235 G>A maps to NM_014014.3 L1418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr16:107121 C>T maps to NM_024571.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:70123624 A>G maps to NM_006857.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr6:7602898 A>G maps to NM_152551.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:41257325 G>T maps to NM_004596.4 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr18:19202684 G>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr15:25223421 C>A maps to NM_022805.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr8:121644767 C>T maps to NM_021021.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr8:121706116 C>T maps to NM_021021.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:51363289 G>T did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr8:51621484 G>T maps to NM_018967.2 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:1079262 G>T maps to NM_018968.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr15:64422134 C>A maps to NM_003099.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr15:64422220 C>G maps to NM_003099.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr17:46196334 G>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:70288145 G>T did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:17915136 A>T maps to ENST00000417048 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:17930107 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:86227557 G>A maps to NM_153816.3 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:64800003 C>T maps to NM_013306.4 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:53815434 G>A maps to NM_052870.2 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:130784448 G>A maps to NM_014758.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:122337128 C>A maps to ENST00000395451 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:186209225 G>A maps to NM_031953.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr8:101661694 C>T maps to NM_152628.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:65618268 G>C maps to NM_152760.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:65620198 C>T maps to NM_152760.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr3:125216803 G>C maps to NM_003794.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr7:2297029 G>C maps to NM_013321.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:2296507 C>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:158327174 G>A maps to NM_016224.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr6:158357062 G>T maps to NM_016224.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr6:158358488 G>C maps to NM_016224.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr6:158318004 C>A maps to NM_016224.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:107955307 C>T maps to NM_018013.3 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:107956399 G>A maps to NM_018013.3 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr12:93968891 C>T maps to NM_003877.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:76354522 C>T maps to NM_003955.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr14:55510556 G>T maps to NM_199421.1 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:46985977 C>A maps to NM_144949.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr18:67992779 C>A maps to NM_004232.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr21:34931600 G>A maps to NM_138927.1 S2129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:97194427 G>A maps to NM_001034954.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:97135750 C>T maps to NM_001034954.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:97170423 G>C maps to NM_001034954.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr10:97098985 C>A maps to NM_001034954.1 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr4:186578703 G>T maps to ENST00000355634 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr4:186510908 C>T maps to ENST00000355634 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr4:186544782 G>A maps to ENST00000355634 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr4:186545037 G>A maps to ENST00000355634 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:22414360 G>A maps to NM_005775.4 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:22414363 C>T maps to NM_005775.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:22421833 G>C maps to NM_005775.4 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:108437113 G>A maps to NM_001013031.1 L597L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-21-5786-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:108366959 A>T maps to NM_001013031.1 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:108430993 C>G did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr10:108536393 T>C maps to NM_001013031.1 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:106960915 G>A maps to NM_014978.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:107005328 C>A maps to NM_014978.1 S966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr10:106907388 C>T maps to NM_014978.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:45332619 C>T maps to NM_003104.5 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr11:121485764 G>T did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr11:121391473 G>A maps to NM_003105.5 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr1:109883448 G>A maps to NM_002959.4 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr1:109884722 G>A maps to NM_002959.4 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr1:109910037 T>A maps to NM_002959.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:39240651 T>A maps to NM_005633.3 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr14:50623786 T>A maps to NM_006939.2 K663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:50671112 C>A maps to NM_006939.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr13:112722244 C>A maps to NM_005986.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr1:204092244 C>T maps to ENST00000367206 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:137484072 C>T maps to NM_004189.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:137483940 C>G maps to NM_004189.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr8:55371730 C>A maps to NM_022454.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr8:55372455 T>C maps to NM_022454.3 H382H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr20:62680533 G>A maps to NM_018419.2 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:139586694 C>T did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr23:139586834 C>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:139587161 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:23893869 C>T maps to NM_006940.4 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:23699315 T>A maps to NM_006940.4 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr12:23728733 G>A maps to NM_006940.4 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:16010542 C>A maps to NM_001145819.1 G669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr11:15994597 A>C maps to NM_001145819.1 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:16068080 C>G maps to NM_001145819.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr16:1034911 G>T maps to NM_014587.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:231405711 G>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:231077722 C>T maps to NM_080424.2 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:231157412 G>A maps to NM_007237.4 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:231256844 C>T maps to NM_138402.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:46005108 C>T maps to NM_003110.5 C587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr2:174820741 G>A maps to NM_003111.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr7:21469887 G>T maps to NM_003112.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:21468912 C>T maps to NM_003112.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr7:21469530 C>T maps to NM_003112.3 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:88769250 A>C maps to NM_030960.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr6:88768509 A>G maps to NM_030960.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr8:7721033 C>T maps to NM_001081552.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:214878801 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:214181976 A>C maps to NM_024532.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:215274862 G>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:214878776 C>A maps to NM_024532.3 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:214204973 A>G maps to NM_024532.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:118554982 G>T maps to NM_206996.2 R1434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:118554859 G>A maps to NM_206996.2 Q1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:118640416 C>T maps to NM_206996.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:118506561 G>A did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr1:118514562 G>C maps to NM_206996.2 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:118548174 A>T maps to NM_206996.2 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:118530768 T>C maps to NM_206996.2 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr1:118558587 C>A maps to NM_206996.2 T1429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr20:34204066 G>T maps to NM_003116.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr20:34203978 C>A maps to NM_003116.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr17:26906444 C>T maps to NM_006461.3 Q981Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:4863818 G>A maps to NM_004890.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr17:49197942 G>A maps to ENST00000376407 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr7:123594319 C>G maps to NM_001174046.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:123593689 G>A maps to NM_001174046.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr23:140336530 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:144337189 G>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:144337226 C>A did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr23:144329180 G>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:144329161 C>T did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:144337260 C>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:142795237 G>A did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:142795315 G>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:142795396 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:142795232 G>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:142795310 G>T did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr23:142795446 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:142795488 T>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:142803732 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:142795456 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:142596771 C>T did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:142596755 C>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:52825620 C>A did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr23:52825600 G>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:52825662 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:172634133 C>T maps to NM_031955.5 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:172835143 C>T maps to NM_031955.5 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:218036153 A>G maps to NM_138796.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:217842373 G>C did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:52928469 C>A maps to NM_145263.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:52948572 C>A maps to NM_145263.2 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:48522386 C>T maps to NM_006038.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:16727235 G>T maps to NM_198546.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr4:124177256 G>A maps to NM_145207.2 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr1:48771546 C>A maps to NM_019073.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr1:48771546 C>A maps to NM_019073.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr14:88892719 G>T maps to NM_018418.4 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr14:88895790 C>T maps to NM_018418.4 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr15:97327380 A>C did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr15:97326899 G>A maps to NM_173499.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:44328257 C>A maps to NM_145026.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:52740665 A>T maps to NM_014041.3 K82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr4:177248311 G>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr6:34508829 C>A maps to NM_012391.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr11:64940228 C>T maps to NM_001008778.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:64939435 C>T maps to NM_001008778.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:99914721 C>T maps to NM_001004351.4 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:99917382 C>T maps to NM_001004351.4 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:35806981 C>T maps to NM_024867.3 F1728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr5:35694424 A>T maps to NM_024867.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr5:35740019 G>T did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr5:35644569 G>A maps to NM_024867.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:220346037 C>T maps to NM_005876.4 I1794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:220337642 C>T maps to NM_005876.4 H1324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:220354142 C>A maps to NM_005876.4 T2801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:220346140 C>A maps to NM_005876.4 R1829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr17:7324848 C>A maps to NM_199339.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:16261935 C>T maps to NM_015001.2 F3067F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:16256433 C>A maps to NM_015001.2 V1233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:16256689 C>T maps to NM_015001.2 Q1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:16257903 A>T maps to NM_015001.2 S1723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:69238584 C>T maps to NM_145658.3 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr15:69238496 A>T maps to NM_145658.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:44890864 C>A maps to NM_025137.3 E1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:44920875 G>C maps to NM_025137.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr13:36909558 G>A maps to NM_001142294.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr15:65273354 C>A maps to NM_016630.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:89598910 C>T maps to NM_003119.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:74382929 C>T maps to NM_182965.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:49131268 G>C maps to NM_020126.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:228884578 G>A maps to NM_001142644.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:228882713 G>T maps to NM_001142644.1 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr2:228892256 G>T maps to NM_001142644.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:228882359 C>T maps to NM_001142644.1 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:47397208 G>A maps to NM_001080547.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:101876640 G>T maps to ENST00000299272 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:62570652 C>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:62570673 T>G did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:62570235 T>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:62570028 C>T did not map to a codon.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr5:147661773 T>A maps to NM_001040129.2 C72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr4:57686745 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr5:147481343 G>T maps to NM_001127698.1 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr5:147693697 G>A maps to NM_032566.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr18:12463418 G>T maps to NM_001128626.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:12506583 C>T maps to NM_001128626.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr18:12449638 A>G maps to NM_001128626.1 *757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr16:89924791 C>T maps to NM_032451.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr16:89920892 A>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:29675657 C>A maps to NM_003123.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr16:28986618 C>T maps to NM_032038.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr16:28995151 G>T maps to NM_032038.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr16:28994514 C>T maps to NM_032038.2 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:55906897 T>C maps to ENST00000371258 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr20:55908749 C>A maps to ENST00000371258 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:32259484 C>T maps to NM_144569.4 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr4:167833818 G>T maps to NM_016950.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr11:14280883 C>A maps to NM_006108.2 C516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr17:47688716 C>A maps to NM_003563.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:139310248 G>T maps to NM_001001664.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr2:139326625 A>T maps to NM_001001664.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:88902859 C>T maps to NM_001040058.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:234969102 G>T maps to NM_006944.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr19:2334701 G>T maps to NM_152988.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr19:2351492 C>T maps to NM_152988.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr19:2345326 C>T maps to NM_152988.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:2337593 C>A maps to NM_152988.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr12:121206827 G>A maps to NM_139015.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:73115536 C>T maps to NM_003124.4 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:73118644 C>T maps to NM_003124.4 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr2:73118539 A>G maps to NM_003124.4 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr15:38591691 G>T maps to NM_152594.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:38885281 G>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr19:38882629 G>A maps to NM_001042522.1 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:155004225 C>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:155003643 G>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:155003857 G>T did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:155003825 G>T did not map to a codon.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr23:155003878 C>T did not map to a codon.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr23:155003873 G>T did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr12:53473102 C>G maps to NM_032840.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr11:55657501 C>A maps to NM_032681.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr11:55655542 T>A maps to NM_032681.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr11:55658945 G>A maps to NM_032681.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr11:55658882 T>C maps to NM_032681.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr16:1827784 G>A maps to NM_080861.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:158583512 C>T maps to NM_003126.2 G2329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr1:158609466 A>G maps to NM_003126.2 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr1:158617399 C>T maps to NM_003126.2 Q1275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:158653175 G>T maps to NM_003126.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr1:158646058 C>T maps to NM_003126.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:158614074 G>T maps to NM_003126.2 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:158615048 G>A maps to NM_003126.2 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr1:158623134 G>A maps to NM_003126.2 F1039F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:158613163 C>A maps to NM_003126.2 E1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:158651324 C>A maps to NM_003126.2 G175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:158648258 G>T maps to NM_003126.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr1:158596724 G>A maps to NM_003126.2 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:158651387 A>G maps to NM_003126.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:158655086 C>T maps to NM_003126.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:158585058 G>T maps to NM_003126.2 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr9:131374419 G>A maps to NM_001130438.2 Q1646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:131383447 G>A maps to NM_001130438.2 K1915K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr9:131345471 C>A maps to NM_001130438.2 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:65236400 G>T maps to ENST00000389723 I1952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr14:65259872 C>T maps to ENST00000389723 Q840Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr14:65249148 G>A maps to ENST00000389723 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:65246616 C>T maps to ENST00000389723 E1437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr14:65263340 C>A maps to ENST00000389723 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr14:65246547 G>A maps to ENST00000389723 I1460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:65246466 G>A maps to ENST00000389723 I1487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr14:65262275 C>A maps to ENST00000389723 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr14:65253721 C>T maps to ENST00000389723 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:65246546 C>A maps to ENST00000389723 E1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:54876328 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:54853175 C>T maps to NM_003128.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:54859734 C>A maps to NM_003128.2 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:54856313 G>T maps to NM_003128.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr2:54856703 C>G maps to NM_003128.2 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:66457281 G>A maps to NM_006946.2 A1981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr11:66463959 C>A maps to NM_006946.2 E1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr19:40993679 C>T maps to NM_020971.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr19:41040048 C>T maps to NM_020971.2 G1386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr19:41074149 C>T maps to NM_020971.2 S2306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:41060525 G>T maps to NM_020971.2 A1686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:41076416 C>A maps to NM_020971.2 R2368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr15:42158428 T>A did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr9:94812282 C>A maps to NM_006415.2 G283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr20:13090813 A>G maps to NM_018327.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr20:13074195 T>C maps to NM_018327.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:18637424 G>T maps to NM_194285.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:79617056 C>A maps to NM_032567.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:142735214 T>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:142741337 G>C did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:142775290 G>C maps to NM_001080415.1 *1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:45832511 T>A maps to NM_018079.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr2:45704185 T>A maps to NM_018079.4 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:30722076 A>T maps to NM_006662.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr16:30719026 G>T maps to NM_006662.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr16:30715392 G>A maps to NM_006662.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:36714568 C>A maps to NM_025248.2 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:36708244 C>A maps to NM_025248.2 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr17:36704852 G>A maps to NM_025248.2 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:6668312 A>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:6652020 G>A maps to NM_001047.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr2:31754472 C>T maps to NM_000348.3 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr22:42300913 C>T maps to NM_004599.2 P1047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr22:42290906 A>T maps to NM_004599.2 K821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:64377731 C>T maps to NM_020762.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:64436625 G>A maps to NM_020762.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr1:206634437 G>A maps to ENST00000414359 Q886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr1:206619561 C>T maps to ENST00000414359 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr3:9036100 C>T maps to NM_014850.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr20:62173648 G>T maps to NM_080823.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr4:57357605 A>G maps to NM_006947.3 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr4:57361543 G>A maps to NM_006947.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:133525543 C>T maps to NM_021203.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:38024092 G>C did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:38020264 T>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:38008973 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:99920282 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:99924319 C>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:99917333 C>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:2819117 T>C maps to NM_016333.3 S2618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:2815494 G>T maps to NM_016333.3 E1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr16:2816579 C>T maps to NM_016333.3 R2017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr16:2819034 C>T maps to NM_016333.3 R2591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:2814713 G>A maps to NM_016333.3 G1395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:2818168 C>G maps to NM_016333.3 S2547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:75894702 C>A maps to ENST00000388802 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:119419692 G>A maps to NM_194286.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr12:119583442 G>C maps to NM_194286.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr20:629440 C>A maps to NM_080725.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr24:2655256 G>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr20:60738678 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:182766614 G>T maps to NM_001130445.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr2:182780262 G>A maps to NM_001130445.1 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:109210856 C>A maps to NM_018984.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr12:109201449 C>A maps to NM_018984.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:27958649 C>A maps to NM_033389.2 E1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr11:67079324 C>T maps to NM_017857.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr9:140083605 G>A maps to NM_003731.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:149489694 C>T maps to NM_198455.2 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:149508025 G>A maps to NM_198455.2 Q3143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:149512314 C>T maps to NM_198455.2 S3548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr7:149486367 G>A maps to NM_198455.2 P1449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:149515738 A>T did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:149475963 T>C maps to NM_198455.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:149489486 G>C maps to NM_198455.2 G1881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr7:149500665 C>T maps to NM_198455.2 S2690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:149478002 C>T maps to NM_198455.2 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:155989840 G>A maps to ENST00000368312 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:57102588 C>A maps to NM_003146.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:65338991 A>T maps to NM_006396.1 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr22:37602606 C>G maps to NM_001051.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr22:37603374 T>A maps to NM_001051.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr22:37603527 G>T maps to NM_001051.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr20:23016629 G>A maps to NM_001052.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr20:23016992 C>T maps to NM_001052.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr16:1129326 G>T maps to NM_001053.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:48116704 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:48123280 C>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:48207010 G>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:48270301 G>C did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:48047123 C>A did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:48047125 C>G did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:52681326 A>G did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:52677350 T>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:52679418 T>C did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:52681965 G>C did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr22:41222544 C>A maps to NM_003932.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:130064580 C>T maps to NM_021978.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:53084598 T>C maps to NM_014682.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:53079508 C>T maps to NM_014682.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr15:80191278 G>C maps to NM_001100880.2 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr8:134478270 C>A maps to NM_173344.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:126278333 A>C maps to ENST00000356132 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:86075210 C>A maps to NM_003896.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr2:86090518 T>A maps to NM_003896.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:86090576 C>T maps to NM_003896.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:98512602 T>A maps to ENST00000493584 *385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:8737259 G>A maps to NM_005418.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr11:8751740 C>A maps to NM_005418.3 G366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr11:8751699 G>A maps to NM_005418.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:107450570 A>G maps to NM_001142351.1 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:107459968 C>T maps to NM_001142351.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:74623246 C>T maps to NM_018414.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr17:74622816 G>T maps to NM_018414.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:76877854 C>T maps to NM_152996.2 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr9:130653124 C>G maps to NM_013443.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:116739882 A>T maps to ENST00000323984 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr12:22487150 G>T maps to NM_003034.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr12:22354569 G>T maps to NM_003034.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:55024413 C>T maps to NM_015879.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr18:55021654 C>T maps to NM_015879.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr18:55020254 C>A maps to NM_015879.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr18:55027339 A>G maps to NM_015879.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr18:55027477 C>G maps to NM_015879.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr18:55020103 C>A maps to NM_015879.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr18:55024482 C>T maps to NM_015879.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr18:44284605 C>A maps to NM_013305.4 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:17363176 G>A maps to NM_001004470.1 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr10:17432597 C>A maps to NM_001004470.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr10:17432597 C>A maps to NM_001004470.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr10:17363098 C>T maps to NM_001004470.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:52556434 G>A maps to NM_015136.2 L2185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr3:52538510 C>G maps to NM_015136.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:52544006 G>A maps to NM_015136.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr3:52538858 G>T maps to NM_015136.2 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr12:104033909 G>T maps to NM_017564.9 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr12:104056673 C>G maps to NM_017564.9 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr12:104097021 A>C maps to NM_017564.9 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:104089512 A>T did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr12:104077059 C>A maps to NM_017564.9 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:104100622 G>A maps to NM_017564.9 G1350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr12:104054498 G>A maps to NM_017564.9 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr12:104149393 G>A maps to NM_017564.9 V2295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr12:104089528 G>T maps to NM_017564.9 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr12:104089552 C>T maps to NM_017564.9 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:104067754 C>A maps to NM_017564.9 C814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr12:104077059 C>A maps to NM_017564.9 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:104089338 A>T maps to NM_017564.9 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:36587756 C>A maps to NM_003149.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr3:136221538 G>A maps to NM_005862.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:136117635 C>T maps to NM_005862.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:136076677 C>T maps to NM_005862.2 E983E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:123224531 C>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:123196826 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:123224560 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:123205134 A>G did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:123197733 G>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:123205066 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:123164846 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:123227994 G>C did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr7:99796199 C>T maps to NM_012447.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr7:99786583 C>A maps to NM_012447.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr7:99779814 G>A maps to NM_012447.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr7:99795707 A>G did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr7:99798771 T>G maps to NM_012447.2 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr7:66774572 G>T maps to NM_022906.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr10:17742235 A>T maps to NM_003473.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr10:17730043 G>T maps to NM_003473.2 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:74087235 G>A maps to NM_213622.1 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:4333704 C>A maps to ENST00000314714 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:4329998 G>A maps to ENST00000314714 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:110835664 C>T maps to NM_139164.1 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:67937246 G>T did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:67943850 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:67940890 G>A did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:67937403 G>C did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:67937590 G>T did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:67938351 C>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:67937292 C>A did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:67938339 C>T did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:67940188 T>C did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr23:67942419 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:67936269 G>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:191862685 G>T maps to NM_007315.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:191849038 G>T maps to NM_007315.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr12:56737277 C>T maps to NM_005419.3 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr17:40474454 G>C maps to NM_139276.2 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:191934479 G>T maps to NM_003151.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr20:47770588 T>C maps to NM_017453.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr8:74464339 G>T maps to NM_001164380.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:23709835 C>A maps to NM_003155.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:89791271 G>A maps to ENST00000433102 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:89793810 C>T maps to ENST00000433102 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr7:89861916 G>A maps to NM_152999.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:120012354 C>T maps to NM_182915.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr7:87912144 A>G maps to NM_024636.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr17:44076725 C>T maps to NM_001007532.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr1:47765601 G>A maps to NM_001048166.1 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:47755240 C>A maps to NM_001048166.1 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:4091352 C>T maps to NM_003156.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:4104114 G>T maps to NM_003156.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:4104505 G>T maps to NM_003156.3 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr4:27000892 G>A maps to ENST00000382009 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:63963137 C>T maps to ENST00000358794 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr19:1218442 G>A maps to NM_000455.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:220462643 C>T maps to NM_052902.2 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:220466707 A>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:220478474 G>T maps to NM_052902.2 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr7:23757097 A>G did not map to a codon.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr4:5418611 G>T maps to NM_018401.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr4:5170130 C>T maps to NM_018401.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr10:134121178 C>A maps to NM_173575.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:8486318 G>T maps to NM_030906.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr20:2097909 C>A maps to NM_080836.3 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr20:2083901 C>T maps to NM_080836.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:219562285 C>T maps to NM_015690.3 I954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr20:43623802 G>T maps to NM_006282.2 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr20:62275231 G>A maps to NM_015894.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr20:62275621 G>T maps to NM_015894.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr8:27098711 G>C maps to NM_030795.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:48808053 C>T maps to NM_172311.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:48808749 A>T maps to NM_172311.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr14:81744700 C>T maps to NM_033104.2 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr10:70644922 T>A maps to NM_001130161.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:70644836 C>A maps to NM_001130161.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr7:134925437 G>A maps to NM_182489.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr12:16052958 G>C maps to ENST00000025399 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:125941311 T>C maps to NM_018387.4 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr9:125898704 G>A maps to NM_018387.4 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:43895469 T>C maps to NM_153700.2 E1505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr15:43903131 C>T maps to NM_153700.2 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr15:43896212 T>A maps to NM_153700.2 P1452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:37085107 A>T maps to NM_003162.2 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr19:47230798 G>C maps to NM_001039877.1 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:7177620 A>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:7223185 A>G did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:7177395 G>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:7268227 C>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:7268041 G>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:7223132 C>T did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:7177574 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:125472275 C>T maps to NM_152713.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr11:125472287 G>A maps to NM_152713.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:13255226 G>C maps to NM_003765.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr20:57251322 C>G maps to NM_001001433.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:57242622 A>G maps to NM_001001433.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr12:131311739 G>A maps to NM_194356.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr11:62595043 G>A maps to NM_003164.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:132785133 G>A maps to NM_003569.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr9:130430388 G>T maps to NM_003165.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr1:109319045 G>C did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:147685232 A>G maps to NM_001127715.1 A1004A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr6:147636665 T>G maps to NM_001127715.1 L473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:120977892 G>T maps to NM_014980.2 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:121137265 C>G maps to NM_014980.2 G1127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:10786661 G>A maps to NM_018423.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr12:10782145 C>A maps to NM_018423.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:104353391 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:104352369 C>A maps to NM_016169.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:46307535 G>A maps to NM_001161841.1 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr20:46313279 G>T maps to NM_001161841.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr20:46365468 G>C maps to NM_001161841.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:48387012 G>A maps to NM_003167.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:48386954 G>T maps to NM_003167.3 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr3:4494691 A>G maps to NM_182760.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:56141874 C>A maps to ENST00000395437 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr20:31577455 C>A maps to NM_080675.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr20:31590417 C>G maps to NM_080675.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:31592073 G>T maps to NM_080675.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr20:31590676 G>A maps to NM_080675.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr12:56398186 G>C maps to NM_001032387.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr12:56397817 C>T maps to NM_001032387.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:21831641 G>A maps to NM_007192.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:21834656 G>T maps to NM_007192.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr6:44971457 G>A maps to NM_181356.1 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:39950219 C>G maps to NM_003169.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:39955613 G>A maps to NM_003169.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:27016512 C>T maps to NM_003170.3 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr17:27011602 G>T did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr17:27009986 A>G maps to NM_003170.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:27009835 C>T maps to NM_003170.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr10:70960233 G>A maps to NM_003171.3 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr10:70960209 C>T maps to NM_003171.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr9:136234198 G>A maps to NM_033161.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr9:136234303 C>T maps to NM_033161.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr9:95846983 G>T maps to NM_145006.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:33195274 T>C maps to NM_015551.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr23:48564682 C>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:48558929 A>G did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr10:14939353 C>A maps to NM_001193424.1 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr10:14939358 C>G maps to NM_001193424.1 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr11:67925194 G>T maps to NM_017635.3 S873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr19:55853360 C>A maps to NM_032701.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr17:30315404 G>T maps to NM_015355.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr15:91795122 C>A maps to NM_014848.4 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:91795650 C>A maps to NM_014848.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr5:75427859 C>T maps to NM_014979.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:113170640 G>A maps to ENST00000374463 F2416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr9:113191429 C>A maps to ENST00000374463 G1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr9:113228154 A>G maps to ENST00000374463 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr9:113170733 G>A maps to ENST00000374463 T2385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr10:29813478 C>A maps to NM_021738.2 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr10:29812614 G>T maps to NM_021738.2 Y976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:109306388 C>T maps to NM_018711.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:9759833 C>A maps to NM_015055.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:115399273 T>C maps to NM_003176.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr1:115438084 T>C maps to NM_003176.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:58475291 A>G maps to NM_014258.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr20:58440890 G>A maps to NM_014258.2 F1450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:15224644 G>A maps to NM_033025.4 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr1:85634813 C>T maps to NM_032184.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:85624808 G>C maps to NM_032184.1 S1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr9:93636954 C>A maps to NM_003177.5 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr9:93639978 C>T maps to NM_003177.5 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:46318943 C>T maps to NM_004819.2 A1233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:46328428 C>A maps to NM_004819.2 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:46328446 C>T maps to NM_004819.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:46338487 T>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:46355781 C>G maps to NM_004819.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:46355644 T>C did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr19:46351142 G>A maps to NM_004819.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr19:46320220 G>A maps to NM_004819.2 Y1031Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:47478794 G>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:47464426 C>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr3:12192810 C>T maps to NM_133625.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:152765647 G>A maps to NM_182961.2 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:152665275 G>T maps to NM_182961.2 V4055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:152708430 T>A maps to NM_182961.2 K2755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr6:152668192 C>A did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr6:152730771 G>A maps to NM_182961.2 V2101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:152647159 A>T maps to NM_182961.2 L5124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:152638028 T>C maps to NM_182961.2 A5555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:152565698 C>A maps to NM_182961.2 P6555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:152779984 C>T maps to NM_182961.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:152763320 C>T maps to NM_182961.2 A1299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr6:152762405 C>A did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr6:152949430 C>A maps to NM_182961.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr6:152665305 C>A maps to NM_182961.2 L4045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:152861156 C>A did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr6:152734569 A>G maps to NM_182961.2 D2049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:152782734 G>T maps to NM_182961.2 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:152712635 C>A maps to NM_182961.2 E2594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr6:152718076 A>G maps to NM_182961.2 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:152614875 C>T maps to NM_182961.2 E5953E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:152831422 C>T maps to NM_182961.2 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr6:152777170 T>C maps to NM_182961.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr6:152671349 C>A maps to NM_182961.2 E3952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr6:152546945 A>C maps to NM_182961.2 A7087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:152560736 C>G maps to NM_182961.2 L6666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr6:152841635 C>A maps to NM_182961.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr6:152737883 A>G maps to NM_182961.2 S1896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr6:152476140 C>G maps to NM_182961.2 L8005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr6:152770761 G>C maps to NM_182961.2 S1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:152629662 A>G maps to NM_182961.2 S5769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:152697610 G>A maps to NM_182961.2 Q3077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr6:152527419 C>T maps to NM_182961.2 S7634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:64483249 G>A maps to NM_182914.2 Q1596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:64540701 C>T maps to NM_182914.2 Q3572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr14:64450531 A>G maps to NM_182914.2 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr14:64593055 A>C maps to NM_182914.2 T4522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr14:64568745 G>T maps to NM_182914.2 G4160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr14:64522938 C>G maps to NM_182914.2 S3341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:64461904 C>T maps to NM_182914.2 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr14:64488572 A>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:64519091 A>T maps to NM_182914.2 K2821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr14:64593521 C>A maps to NM_182914.2 Y4638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr14:64610581 G>A maps to NM_182914.2 K5133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:64688334 G>T maps to NM_182914.2 A6701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr6:33405911 C>T maps to NM_006772.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:33393612 C>T maps to NM_006772.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr6:33405596 C>A maps to NM_006772.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr16:2042733 G>T maps to NM_004209.5 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr19:48878903 C>A maps to NM_012451.3 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:34053868 G>A maps to NM_003895.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr21:34029362 T>C maps to NM_003895.3 P882P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr21:34003385 C>A maps to NM_003895.3 P1586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr15:99670661 C>T maps to ENST00000336292 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr15:99672068 C>T maps to ENST00000336292 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr15:99673094 G>T maps to ENST00000336292 G1509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr5:150028163 G>T maps to NM_001166209.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:150028852 C>G maps to NM_001166209.1 S583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr4:119948591 A>G maps to NM_133477.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:75407378 C>G maps to NM_001114133.1 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr3:63601156 A>G maps to NM_001130003.1 *286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr17:35913321 G>A maps to NM_007247.4 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:35931927 C>A maps to NM_007247.4 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:49055481 C>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr12:79693309 G>T maps to NM_005639.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr12:33560268 G>A maps to NM_198992.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr12:33579078 G>T maps to NM_198992.3 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:155838212 A>G maps to NM_152280.4 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:155838147 G>T maps to NM_152280.4 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr11:66807556 G>T maps to NM_001177880.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:45268003 G>A maps to NM_020826.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:45274067 G>A maps to NM_020826.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:210334197 A>G maps to NM_001146261.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:210334353 A>G maps to NM_001146261.1 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:210126102 T>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:210273456 C>G maps to NM_001146261.1 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:46968610 G>A maps to NM_031912.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:62462805 G>T maps to NM_031914.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr14:62547934 G>A maps to NM_031914.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:19195300 C>T maps to NM_016524.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:202572183 C>T maps to NM_177402.4 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:202574735 T>G maps to NM_177402.4 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:202571624 C>A maps to NM_177402.4 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:51128807 C>T maps to NM_001160329.1 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr19:51132550 C>T maps to NM_001160329.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr18:40850347 G>A maps to NM_020783.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr18:40850569 G>T maps to NM_020783.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:55687075 C>T did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr11:61290738 G>T maps to NM_004200.2 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:7324381 C>T maps to NM_175733.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr11:7334799 G>A maps to NM_175733.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:7334649 C>T maps to NM_175733.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:85415984 T>C maps to ENST00000359152 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr11:85445044 C>A maps to NM_001162953.1 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr11:85418531 G>T maps to ENST00000359152 G1527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr11:85445731 T>A maps to NM_001162953.1 K214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:159146620 C>A maps to ENST00000297239 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:99945579 G>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:99956579 T>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:99955934 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:37913507 G>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:37913588 T>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:37961664 G>A did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:37984549 G>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:37913574 C>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:37953620 G>C did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:37953629 C>A did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:37969624 T>A did not map to a codon.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr23:37967888 G>A did not map to a codon.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr23:37965891 A>G did not map to a codon.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr11:64895952 C>T maps to NM_172230.2 E585E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:166576076 C>G maps to NM_003181.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:166580193 C>T maps to NM_003181.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:132966854 A>G maps to NM_138327.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:132967046 G>C maps to NM_138327.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr6:132939032 C>A maps to NM_001033080.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr6:132910357 C>A maps to NM_003967.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr6:132910450 G>T maps to NM_003967.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:132891843 C>T maps to NM_175067.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:132891933 C>T maps to NM_175067.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:132892143 G>A maps to NM_175067.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr6:132891741 G>A maps to NM_175067.1 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:132891789 C>A maps to NM_175067.1 C110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:132874418 C>T maps to NM_053278.1 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:132874079 T>A maps to NM_053278.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr6:132859710 G>T maps to NM_175057.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:149699962 A>G maps to NM_015093.4 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr6:149700430 G>A maps to NM_015093.4 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:30872796 G>T did not map to a codon.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr23:30873660 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:30849552 C>T did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:30873080 T>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:30873248 G>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:30872849 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:97363036 G>A maps to NM_003182.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:123846007 G>A maps to NM_206862.2 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:123845053 G>A maps to NM_206862.2 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr10:123970464 G>A maps to NM_206862.2 T2175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr4:1730121 G>C maps to NM_006342.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:75276593 C>A maps to NM_001058.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr10:71168821 G>A maps to NM_001057.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr4:104511075 G>T maps to NM_001059.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr4:104577501 C>G did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr4:104640739 C>A maps to NM_001059.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:166829462 G>A maps to NM_053053.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:70613228 C>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:70603820 C>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:70621430 C>G did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:70612493 G>A did not map to a codon.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr23:70603898 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:70597476 G>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:70674029 T>A did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:70602910 A>C did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:70598701 G>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:70603812 T>C did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr23:70678144 G>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr23:70597468 G>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:70601651 G>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr16:84218552 G>A maps to NM_005679.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr16:84214990 C>A maps to NM_005679.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:32631620 C>T maps to NM_153809.2 E1319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:32631521 C>A maps to NM_153809.2 V1352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr9:32630257 C>A maps to NM_153809.2 E1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr9:32635550 C>T maps to NM_153809.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:120797487 G>A maps to NM_003184.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr8:120754866 G>A maps to NM_003184.3 R1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr8:120774747 A>T maps to NM_003184.3 L822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr10:7860770 C>T maps to NM_031923.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:8007023 C>A maps to NM_031923.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr10:7860716 G>T maps to NM_031923.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr10:7866290 A>T maps to NM_031923.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr10:8055794 C>G maps to NM_031923.2 Y890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:60589752 G>T maps to NM_003185.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr20:60578820 C>T maps to NM_003185.3 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr20:60578310 G>A maps to NM_003185.3 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr18:23895362 G>C did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr18:23895264 A>G maps to ENST00000418698 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr10:105147935 C>A maps to NM_006951.3 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:229730433 C>T maps to NM_014409.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:229730376 G>A maps to NM_014409.3 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:99711546 G>T maps to ENST00000472509 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:99711347 G>A maps to ENST00000472509 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr23:100547910 G>T did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:100530213 T>C did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:100530222 T>G did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:77393467 G>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:159889625 C>A did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:47691493 C>A maps to ENST00000371883 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:160035486 C>T maps to NM_033394.2 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr2:160031615 G>A maps to NM_033394.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:160076236 G>A maps to NM_033394.2 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr17:61432616 G>A maps to ENST00000389520 Q742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr17:61492926 C>A maps to ENST00000389520 Y1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:162087606 G>T maps to NM_004180.2 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:162088004 T>A maps to NM_004180.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:162088021 C>G maps to NM_004180.2 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:27778619 C>G maps to NM_020791.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:27869856 C>T maps to NM_020791.2 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:27794160 A>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr16:29997771 G>T maps to NM_016151.2 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr16:29997088 G>T maps to NM_016151.2 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:32805734 G>T maps to ENST00000452392 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr6:33281788 C>A maps to NM_172208.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr6:33272136 G>A maps to NM_172208.2 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr4:16189951 A>G maps to NM_153365.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:234563323 T>C maps to NM_005646.3 Q1083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:11077006 A>C maps to NM_007375.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:38299820 C>A maps to ENST00000443402 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:38299745 G>T maps to ENST00000443402 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:150478152 C>T maps to NM_025150.3 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr1:150477402 C>T maps to NM_025150.3 F614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr15:102255119 G>A maps to NM_152334.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr1:6637113 C>A maps to NM_138697.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:6635259 C>T maps to NM_138697.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:6639479 C>T maps to NM_138697.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr1:19168340 A>T maps to NM_152232.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr1:19181213 C>T maps to NM_152232.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr1:19180802 G>A maps to NM_152232.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr5:9629766 G>A maps to NM_019599.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr5:9629814 G>A maps to NM_019599.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:9629529 G>A maps to NM_019599.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr5:9629448 G>T maps to NM_019599.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:122635111 G>A maps to NM_016945.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr7:122635529 G>A maps to NM_016945.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:122635319 C>T maps to NM_016945.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr12:11174582 C>T maps to NM_176888.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:11174552 G>C maps to NM_176888.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr12:11149888 G>A maps to NM_176889.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr12:11286735 G>A maps to NM_001097643.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr12:11183529 C>A maps to NM_176885.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr12:11183142 G>A maps to NM_176885.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:141478588 T>C maps to NM_016944.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr12:11339132 A>G maps to NM_181429.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:11214161 G>T maps to ENST00000422992 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr7:141491033 G>T maps to NM_018980.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr12:10954980 T>C maps to NM_023919.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:10959201 A>G maps to NM_023918.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr20:13463979 A>G maps to NM_017714.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:71602688 G>A maps to NM_000353.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:125531057 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:125531106 C>A maps to NM_032026.3 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:212969881 A>C maps to NM_001146171.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:27868361 G>T maps to ENST00000409980 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:153648061 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:38091725 C>T maps to NM_015173.2 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:38022222 C>T maps to NM_015173.2 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr4:38047523 A>G maps to NM_015173.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:38138812 G>T maps to NM_015173.2 E1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:30688369 G>A maps to ENST00000403477 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr11:67177084 G>T maps to NM_198517.2 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:67171759 C>T maps to NM_198517.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr9:131568187 G>T maps to NM_018201.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr4:6969093 A>G maps to NM_001113361.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr17:77914762 C>T maps to NM_019020.2 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:50385599 C>T maps to NM_024682.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr19:50384663 A>C maps to NM_024682.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:26667969 G>T maps to NM_018317.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr4:26689972 A>T maps to NM_018317.2 K300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:47507499 G>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr6:37284590 G>A maps to NM_017772.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:100034981 T>A maps to ENST00000394144 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:100018090 C>T maps to ENST00000394144 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr3:100018111 C>T maps to ENST00000394144 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:48418068 T>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:48418400 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:48418719 G>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:48418239 A>G did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:28889926 C>T maps to NM_015594.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:75876394 C>T maps to ENST00000431480 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr13:75915718 G>C maps to ENST00000431480 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr13:76055558 C>T maps to ENST00000431480 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:17418095 C>A maps to NM_001134381.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr6:13305332 T>C maps to NM_016495.4 *294W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr2:101646110 G>A maps to NM_001102426.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:106083279 G>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:106108821 C>T did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr23:106082561 G>C did not map to a codon.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr23:106065218 G>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:106046202 G>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:106097467 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:106083926 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:106097493 C>A did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:106111677 A>T did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr4:141543384 C>A maps to NM_015130.2 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr4:141600877 G>C maps to NM_015130.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:179302149 C>T maps to NM_198868.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr5:179297372 G>A maps to NM_198868.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr6:42713445 C>A maps to NM_003192.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:42712980 G>A maps to NM_003192.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr3:186272062 C>T maps to NM_001134415.1 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:80828253 G>A maps to NM_005993.4 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:80897337 C>G maps to NM_005993.4 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr17:80887327 C>T maps to NM_005993.4 H981H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr4:107173141 C>A maps to NM_001163436.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr12:64879293 G>C did not map to a codon.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr3:176769460 G>A maps to NM_024665.4 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:176769496 A>G maps to NM_024665.4 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr24:6893164 C>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr24:6938803 A>T did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr14:55903373 C>T maps to NM_199047.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:162274739 C>T maps to NM_006593.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:162273452 C>T maps to NM_006593.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr11:67402567 C>T maps to NM_005995.4 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:85446756 C>A maps to NM_001080508.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr6:85446510 C>A maps to NM_001080508.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr6:85446864 A>G maps to NM_001080508.1 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr6:85446683 G>A maps to NM_001080508.1 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:85446453 G>T maps to NM_001080508.1 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:85457706 C>A maps to NM_001080508.1 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:168260472 T>C maps to NM_005149.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:168260433 G>T maps to NM_005149.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr17:59483115 C>A maps to NM_005994.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr17:59480531 C>A maps to NM_005994.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr7:35244187 A>G maps to NM_001077653.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr7:35284590 G>A maps to NM_001077653.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr7:35242155 G>T maps to NM_001077653.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr7:35289659 C>A maps to NM_001077653.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr17:45822321 C>T maps to NM_013351.1 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:45822455 G>A maps to NM_013351.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr17:45822500 C>A maps to NM_013351.1 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:79282781 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:79279580 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:79286287 C>T did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr23:79281248 C>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:79277823 C>A did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:79281105 G>C did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:79282233 C>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr23:79286182 A>G did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr23:79278708 G>C did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:79286061 C>A did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr23:79282759 G>C did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:79286002 G>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:79279606 A>T did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:115114127 C>T maps to NM_016569.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:115118750 C>T maps to NM_016569.3 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:115120792 C>T maps to NM_016569.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr12:115120861 G>T maps to NM_016569.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:115117423 G>C maps to NM_016569.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:115114169 G>A maps to NM_016569.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:115118835 G>T maps to NM_016569.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr17:59557522 G>A maps to ENST00000393853 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr12:114837385 C>T maps to NM_000192.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr12:114836485 G>T maps to NM_000192.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr12:114823353 C>A maps to NM_000192.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr12:114836512 G>A maps to NM_000192.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:114841586 C>T maps to NM_000192.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr16:30100410 C>T maps to NM_004608.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr16:30102164 C>T maps to NM_004608.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr7:139715639 G>A maps to NM_001166253.1 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr7:139661860 T>G maps to NM_001166253.1 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:139611110 C>A maps to NM_001166253.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr8:54891623 T>A maps to NM_006756.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr23:101381880 G>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:101382146 G>T did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr23:101382215 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:102864064 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:102864367 C>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:102528981 C>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:101396062 C>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:101396001 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr23:101396086 C>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:13681156 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:24078940 G>A maps to NM_003198.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:24083467 G>T maps to NM_003198.2 G730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr18:44560771 A>T maps to NM_016427.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr18:44555131 G>T maps to NM_145653.3 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr18:44555160 G>T maps to NM_145653.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr18:44554668 C>G maps to NM_145653.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr10:132944775 T>G maps to NM_174937.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr10:133106546 A>C maps to NM_174937.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr10:133106501 C>T maps to NM_174937.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:57458627 C>A maps to NM_207036.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr22:42575681 G>A maps to NM_005650.1 G1894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr6:134210894 G>T maps to NM_003206.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:27373019 G>T maps to NM_175769.2 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:85361183 C>A maps to NM_031283.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr10:114724334 C>T maps to NM_001146274.1 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:152057616 A>T maps to NM_001008536.1 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr1:152059146 T>C maps to NM_001008536.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:152058372 C>T maps to NM_001008536.1 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:152057684 G>A maps to NM_001008536.1 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr12:110340867 C>T maps to NM_032300.4 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr11:67818062 G>T maps to NM_006019.3 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:96152929 G>T maps to NM_004918.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:59620685 T>C maps to NM_001062.3 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr11:59631501 G>T maps to NM_001062.3 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:59626612 A>T maps to NM_001062.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:59631458 G>T maps to NM_001062.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:59623396 C>A maps to NM_001062.3 L294L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-18-3406-01A-01D-0983-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr22:31003381 G>T maps to ENST00000450638 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr6:160200658 C>T maps to NM_030752.2 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr6:167786680 G>A maps to NM_004610.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:35088734 G>T maps to NM_001093728.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr6:44253967 G>A maps to NM_182539.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr6:44249915 G>C maps to NM_182539.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr1:67243029 G>T maps to NM_152665.2 G145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:67243016 G>A maps to NM_152665.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:67220351 C>G maps to NM_152665.2 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr12:104376575 G>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr12:104378654 C>T maps to NM_003211.4 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:115947892 A>T maps to NM_198795.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr10:115970709 T>C maps to NM_198795.1 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr13:61083926 G>T maps to NM_001146070.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:179659938 T>A maps to ENST00000444136 L990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr1:179604968 G>T maps to ENST00000444136 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:179632620 C>T maps to ENST00000444136 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:179604998 C>A maps to ENST00000444136 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr6:46656834 G>T maps to NM_001010870.2 G324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr6:46661522 C>T maps to NM_001010870.2 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:46659203 G>T maps to NM_001010870.2 V1113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:46669615 G>T maps to NM_001010870.2 E2095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr6:46656441 G>T maps to NM_001010870.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:100232919 C>G maps to NM_014290.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:104472877 A>G maps to NM_153046.2 E622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:49846556 C>G maps to NM_003598.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:97854117 G>A maps to ENST00000379795 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr14:102916036 G>C maps to NM_014844.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr4:65180418 T>C maps to NM_001010874.4 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:121028815 C>T maps to NM_005422.2 S1524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr11:120983872 G>T maps to NM_005422.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr11:121058627 C>T maps to NM_005422.2 F2029F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr11:121028737 C>T maps to NM_005422.2 F1498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:121023770 C>A maps to NM_005422.2 S1429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr11:121028812 C>T maps to NM_005422.2 I1523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr11:120996090 C>T maps to NM_005422.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:114043500 G>A maps to NM_058222.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr9:27229208 T>C maps to NM_000459.3 C1118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr17:6718549 G>A maps to NM_053285.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr17:15222446 C>A maps to NM_031898.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:95539829 G>A maps to NM_144705.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr2:95540613 G>A maps to NM_144705.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:95537338 G>T maps to NM_144705.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:95542357 A>G maps to NM_144705.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:10775922 C>A maps to NM_144674.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:1545550 C>T maps to NM_016111.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:53454750 C>T maps to NM_170754.2 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:20864796 G>A maps to NM_007110.4 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr14:20854782 C>G did not map to a codon.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr14:20849730 C>A maps to NM_007110.4 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr14:20852760 G>T maps to NM_007110.4 R1073R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:58010446 C>T maps to NM_199046.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr8:73932952 C>T maps to NM_017489.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr5:1253923 C>T maps to NM_198253.2 K1106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr5:1278881 G>T maps to NM_198253.2 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr7:115891999 G>T maps to NM_015641.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:35606844 G>T maps to NM_006285.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr9:35608435 C>T maps to NM_006285.2 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr9:35609123 G>A maps to NM_006285.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr9:35609288 G>A maps to NM_006285.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:35608408 T>A maps to NM_006285.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:45887416 G>C maps to NM_007170.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:45887416 G>A maps to NM_007170.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:45887496 G>A maps to NM_007170.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:70446378 G>T maps to NM_030625.2 V1773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr10:70446444 T>G maps to NM_030625.2 P1795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr10:70426799 A>C did not map to a codon.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr4:106155422 G>A maps to ENST00000513237 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:74275350 A>T maps to ENST00000409262 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:74300733 G>T maps to ENST00000409262 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:103090162 G>C maps to NM_017746.3 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr9:103066023 C>A maps to NM_017746.3 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:43922078 G>T maps to NM_031451.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:43922124 C>A maps to NM_031451.4 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr19:43910664 G>A maps to NM_031451.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr23:69898678 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:69942542 A>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:69871347 G>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:104464791 G>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:104464162 G>C did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:104464884 G>T did not map to a codon.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr23:104464699 G>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:104464729 G>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:104464649 G>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr23:104464751 G>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr23:104464810 G>C did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:104464312 C>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:107225186 G>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr23:107225169 A>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:107224903 G>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:107225024 C>T did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:56670913 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:30705258 C>T maps to NM_031271.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr8:30702472 A>T maps to NM_031271.3 L1354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:30705225 G>A maps to NM_031271.3 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr8:30703522 A>T maps to NM_031271.3 L1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:30704886 C>T maps to NM_031271.3 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr8:30700807 G>C maps to NM_031271.3 S1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr17:80320049 G>A maps to NM_207459.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr17:62290609 G>C maps to NM_018469.3 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:133494301 G>A maps to NM_001063.3 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:133478160 C>A maps to NM_001063.3 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr10:60147947 A>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr10:60154125 G>A maps to NM_003201.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:50791150 C>A maps to ENST00000263046 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:50740555 C>A maps to NM_172238.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:50682844 C>G maps to NM_172238.3 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr6:50740363 C>A maps to NM_172238.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:50683049 C>G maps to NM_172238.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:50682827 G>C did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr16:4312390 G>T maps to NM_003223.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr6:155635433 C>G maps to NM_016020.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr6:155635541 G>C maps to NM_016020.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr12:51504758 C>A maps to NM_005653.4 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:141682762 C>A maps to NM_001178139.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr3:141697361 C>T maps to NM_001178139.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:141671422 C>A maps to NM_001178139.1 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:132351915 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:48896774 G>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr21:43783370 A>G maps to NM_003225.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr21:43735445 C>T maps to ENST00000291525 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr3:100447601 C>G maps to NM_001007565.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:188361710 G>A maps to NM_006287.4 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr7:100230712 C>A maps to NM_003227.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:133961036 G>T maps to NM_003235.4 G1750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr8:133925454 G>C maps to NM_003235.4 S1441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr8:133961120 T>G maps to NM_003235.4 P1778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:134146938 G>A maps to NM_003235.4 Q2736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr13:95228566 C>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:31488638 C>T maps to NM_001042454.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:218520186 G>A maps to NM_001135599.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr1:218578577 G>A maps to NM_001135599.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:218607482 G>C maps to NM_001135599.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:135388805 C>G maps to NM_000358.2 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr3:30713590 C>T maps to NM_001024847.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:30713391 A>G maps to NM_001024847.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:30713400 G>A maps to NM_001024847.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:92185494 A>T maps to NM_003243.4 C456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:92177901 G>A maps to NM_003243.4 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr2:105889312 G>A maps to NM_004257.4 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr20:35219626 G>A maps to NM_021809.6 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr23:89177511 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:89177592 A>G did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:89177790 A>C did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:89177375 T>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:89177751 C>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr23:89177804 C>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:89177432 A>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:89177497 C>A did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr23:89177747 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:89177475 A>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr14:24724585 G>C maps to NM_000359.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:24723419 G>A maps to NM_000359.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr20:2308907 G>A maps to NM_003245.3 W410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:44935187 G>T did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:44938286 G>T maps to NM_003241.3 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr15:43533123 A>G maps to NM_201631.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr20:2398083 C>T maps to NM_198994.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:2375199 C>A maps to NM_198994.2 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr20:2380259 C>A maps to NM_198994.2 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr20:2398025 C>T maps to NM_198994.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr20:2384443 C>A maps to NM_198994.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr20:2375158 G>A maps to NM_198994.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:43594441 G>A maps to NM_052955.2 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:43571925 G>A maps to NM_052955.2 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:56699596 A>C maps to NM_024831.6 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:56698930 T>C maps to NM_024831.6 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr11:2185534 G>T maps to NM_199292.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr11:2189847 C>T maps to NM_199292.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr20:57564616 G>T maps to NM_198976.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:43804382 T>C did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:43514125 A>G maps to ENST00000330266 P1696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr15:71184575 G>A maps to NM_020147.3 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr4:76447059 C>T maps to NM_144721.4 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr22:21355636 G>A maps to NM_030573.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:83839357 C>T maps to NM_024672.4 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr6:169634880 G>T maps to NM_003247.2 C533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr6:169648706 G>A maps to NM_003247.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:169632818 G>T maps to NM_003247.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr6:169632235 C>A maps to NM_003247.2 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:169641871 C>T maps to NM_003247.2 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:169646361 G>A maps to NM_003247.2 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr6:169650858 C>T maps to NM_003247.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr6:169648982 G>T maps to NM_003247.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr1:155172144 G>A maps to NM_007112.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr1:155171306 C>T maps to NM_007112.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:155175102 C>T maps to NM_007112.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr5:79363824 G>A maps to NM_003248.4 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr19:371312 A>T maps to NM_016585.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:128176331 G>C maps to NM_001164685.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:157158519 G>C maps to NM_017872.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:157159977 G>A maps to NM_017872.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:88484971 C>A maps to NM_018271.3 Y401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr2:88474876 C>A maps to NM_018271.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:88472875 A>G maps to NM_018271.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:88478389 G>A maps to NM_018271.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:122747265 G>A did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:122831591 G>T did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:122757716 G>C did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:122759796 G>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:122840734 C>T did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr23:122846736 G>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:122772853 C>G did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:122757940 A>C did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:122801008 C>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:122754762 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:122757770 A>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:122765632 C>A did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr22:29938945 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:2799763 C>T maps to NM_003249.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:2810339 G>T maps to NM_003249.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:2799757 G>C maps to NM_003249.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:38230775 C>G maps to NM_003250.5 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr1:36755022 C>A maps to NM_005119.3 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:52952154 G>A maps to NM_018676.3 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:52951734 C>G maps to NM_018676.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr13:52952430 G>T maps to NM_018676.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr15:72057525 C>A maps to NM_024817.2 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr15:72039275 G>A maps to NM_024817.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr7:11464332 G>A maps to ENST00000423059 R1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr7:11676274 A>T maps to ENST00000423059 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr7:11486856 C>A maps to ENST00000423059 G934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr7:11468627 A>C maps to ENST00000423059 R1063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr2:137814719 G>C maps to ENST00000272643 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:138330101 G>A maps to ENST00000272643 W1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:137814086 T>A maps to ENST00000272643 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:138400098 G>T maps to ENST00000272643 G1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr2:138163300 C>G maps to ENST00000272643 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:137852568 A>G maps to ENST00000272643 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:39971519 C>A maps to NM_025264.4 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:9426216 G>T maps to NM_015453.2 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:134118799 G>C maps to NM_199298.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:121347732 C>A maps to NM_001033925.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:32638619 G>A maps to NM_003253.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr21:32598069 G>C maps to NM_003253.2 S594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr21:32513670 C>T maps to NM_003253.2 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr6:155577834 C>T maps to ENST00000456144 I1591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr6:155485734 G>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:155504518 A>C maps to ENST00000456144 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr19:4817414 G>A maps to NM_182919.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:43787097 C>T maps to NM_005424.2 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr1:43774786 C>T maps to NM_005424.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:43777782 C>T maps to NM_005424.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:153692075 G>A maps to NM_145720.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:114014419 G>T maps to ENST00000481065 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr3:114026869 G>A maps to ENST00000481065 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr5:156346548 T>C maps to NM_138379.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr12:56817236 G>A maps to NM_003920.3 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr16:4391371 C>T maps to NM_016069.8 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:48752383 C>G did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:7997723 C>G did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr3:12195883 C>A maps to NM_003256.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:32050833 C>T maps to NM_022164.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:156395781 C>G maps to NM_015508.4 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:43471416 C>T maps to NM_001146016.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr6:43472650 C>G maps to NM_001146016.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:30058720 G>A maps to NM_003257.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr15:30024885 G>A maps to NM_003257.3 Q624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr19:3728465 C>T maps to NM_014428.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:3738988 C>T maps to NM_014428.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr19:3740704 C>G maps to NM_014428.1 S629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:53275206 C>A maps to ENST00000423516 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:153556266 G>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr4:164393683 G>A maps to NM_032136.4 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:3028719 G>A maps to NM_003260.4 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr15:70347519 G>A maps to NM_005078.2 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr15:70351754 G>A maps to NM_005078.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr9:82320815 G>T maps to ENST00000376537 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:82323694 A>T maps to ENST00000376537 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:82323124 G>A maps to ENST00000376537 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr2:171863103 G>A maps to ENST00000360843 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr4:167020661 C>A maps to ENST00000507499 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr9:35710608 G>T maps to NM_006289.3 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:63044535 G>A maps to NM_015059.2 Q1414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr15:63084979 G>C maps to NM_015059.2 T1959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr15:63029095 G>T maps to NM_015059.2 T1126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr15:62944322 T>C maps to NM_015059.2 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:63031710 C>T maps to NM_015059.2 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr4:38798564 C>A maps to NM_003263.3 E630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:38775612 G>A maps to NM_030956.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr4:38776272 G>A maps to NM_030956.3 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:38776167 C>A maps to NM_030956.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:154625880 C>T maps to NM_003264.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr4:154624934 T>C maps to NM_003264.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr4:187004693 G>A maps to NM_003265.2 Q618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr4:187004153 G>T maps to NM_003265.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr9:120475752 C>T maps to NM_138554.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr9:120475812 C>A maps to NM_138554.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:120475242 C>A maps to NM_138554.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr9:120476481 A>G maps to NM_138554.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr9:120475456 A>T maps to NM_138554.3 K351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr9:120470890 C>A maps to NM_138554.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr9:120476736 C>T maps to NM_138554.3 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr9:120475353 G>T maps to NM_138554.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr1:223285746 A>C maps to NM_003268.5 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:223285331 G>A maps to NM_003268.5 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:12904134 G>T did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:12905133 A>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:12906212 C>G did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:12905840 G>A did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr23:12904871 C>A did not map to a codon.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr23:12938147 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:12938412 C>T did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:12937336 A>G did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:12939467 A>G did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:12939452 C>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr1:62190774 C>A maps to ENST00000371180 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:102191951 G>C maps to NM_078474.2 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr3:196051167 A>G maps to NM_138461.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:228243942 G>A maps to NM_024795.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:149192699 G>A maps to NM_004617.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:149216508 G>A maps to NM_004617.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr8:105367344 C>T maps to NM_030788.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr8:105367394 G>C maps to NM_030788.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr8:105361463 C>A maps to NM_030788.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr8:105361289 C>A maps to NM_030788.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr8:105361445 C>A maps to NM_030788.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr8:105361136 A>G maps to NM_030788.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr13:100181718 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:98303963 C>T did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr20:30745748 G>A maps to NM_014742.3 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr20:30745598 G>A maps to NM_014742.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr20:30729589 G>T maps to NM_014742.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:219143269 G>A maps to NM_022152.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:50149492 G>T maps to NM_001098576.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr9:75407165 G>A maps to NM_138691.2 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:75431060 T>C maps to NM_138691.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr20:2597738 A>T maps to NM_080751.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr20:2616613 C>G maps to NM_080751.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr20:2560662 C>A maps to NM_080751.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr20:2577826 C>T maps to NM_080751.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr20:2591192 G>T maps to NM_080751.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr20:2575613 G>A did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:81637255 G>T maps to ENST00000454937 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr15:81638753 G>T maps to ENST00000454937 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr16:19475264 C>T maps to NM_001105248.1 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr16:19501869 C>T maps to NM_001105248.1 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr16:19451422 G>C maps to NM_001105248.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:19068004 C>T maps to NM_024847.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:19033092 C>T maps to NM_024847.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr16:19033050 C>T maps to NM_024847.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:129389564 G>A maps to NM_001017395.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr3:129370614 C>T maps to NM_001017395.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr3:129389432 A>T maps to NM_001017395.3 Y417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:205238662 C>T maps to NM_014858.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr13:114203834 G>A maps to NM_017905.4 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:20097875 A>C maps to NM_181719.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:20067392 C>A maps to NM_181719.4 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:68893907 C>A maps to NM_024562.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr16:68936357 A>C maps to NM_024562.1 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:75614414 G>T maps to NM_006827.5 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:124074953 G>T maps to NM_006815.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr15:79603746 C>G maps to NM_007364.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:79606179 C>T maps to NM_007364.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr14:77808182 G>C maps to NM_213601.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:193059100 C>T maps to NM_016192.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr2:193049090 G>T maps to NM_016192.2 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:42089418 G>C maps to NM_032376.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72791232 C>T maps to NM_017728.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72832360 C>T maps to NM_017728.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr17:41368481 C>T maps to NM_145041.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr7:12254525 G>T maps to NM_018374.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr17:8079344 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:133098692 C>T maps to NM_001136469.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:133098899 A>G maps to NM_001136469.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr3:133098893 G>T maps to NM_001136469.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr3:133109123 C>T maps to NM_001136469.1 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:60687195 G>T maps to NM_024092.2 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr12:44782228 C>A maps to NM_032256.1 S440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr12:44770375 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:108985910 G>A maps to NM_181724.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr12:122181596 C>T maps to NM_001080825.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr11:102272391 T>C maps to NM_052932.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:98377351 C>A maps to NM_015348.1 G1639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:98409344 T>A maps to NM_015348.1 P1216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr11:60696321 G>T maps to NM_017870.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:60704149 C>G maps to NM_017870.3 S949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:126139081 G>A maps to NM_052907.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr12:126004171 G>C did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:126138641 C>T maps to NM_052907.2 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr12:126128683 G>C maps to NM_052907.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr12:126004125 C>A maps to NM_052907.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:125834676 G>T maps to NM_052907.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:129558938 G>A maps to NM_133448.2 F927F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr12:129558725 C>T maps to NM_133448.2 E998E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr12:129566321 A>T maps to NM_133448.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr12:129559244 T>C maps to NM_133448.2 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr12:130185001 G>T maps to NM_133448.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr17:32956180 G>C maps to NM_207313.1 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr17:32959859 C>T maps to NM_207313.1 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr17:32955602 G>C maps to NM_207313.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:32956199 C>T maps to NM_207313.1 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr17:32964686 G>T maps to NM_207313.1 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:120198200 C>T maps to NM_001198670.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:142983528 C>T maps to NM_153345.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:48836477 A>G maps to NM_018273.2 *460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:42824507 C>T maps to ENST00000406159 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr19:42818841 C>T maps to ENST00000406159 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:5772892 C>T maps to NM_152784.3 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:5751818 C>T maps to NM_152784.3 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr19:5778596 C>T maps to NM_152784.3 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr19:36037608 G>C maps to NM_032635.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:10725207 G>A maps to NM_016462.3 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:152058441 G>C maps to NM_001123228.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:85826822 C>A maps to NM_001031738.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr11:66062538 C>A maps to NM_153266.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr11:66062454 C>T maps to NM_153266.3 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr4:38972692 T>C maps to NM_024943.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr16:21181807 G>A maps to ENST00000451578 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:109414718 C>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:109414654 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:109388077 T>C did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr1:109637042 T>C maps to NM_020141.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr5:138857015 C>A maps to NM_198282.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:150490334 C>A maps to NM_014020.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:120439363 G>T maps to NM_030577.2 *312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr2:669657 C>T maps to NM_152834.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:148685676 G>T did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:148685677 T>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:148690400 C>A did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr12:72092833 T>C maps to NM_018279.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:15405802 G>A maps to NM_001004320.1 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr7:19765274 G>T maps to NM_152774.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:74332990 G>A maps to NM_013390.2 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:74340562 G>C maps to NM_013390.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr10:95661024 G>T maps to NM_001134658.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr10:95660691 A>G maps to NM_001134658.1 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:130761935 T>C maps to NM_052913.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:130762799 A>G maps to NM_052913.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:9661494 G>C maps to NM_001130924.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr19:11453491 T>A maps to NM_198536.2 *190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:212558648 G>A maps to NM_001198862.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:212583815 G>A maps to NM_001198862.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:212560295 C>A maps to NM_001198862.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr3:190165605 G>T maps to NM_207316.1 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:129813501 G>T maps to NM_032842.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr22:25331383 G>A maps to ENST00000423535 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr22:25331524 G>A maps to ENST00000423535 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:138487699 C>T maps to ENST00000422794 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr2:27260539 C>T maps to NM_017727.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr16:29979361 A>G maps to NM_194280.3 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr17:10628380 C>A maps to NM_001004313.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr1:27648882 G>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr10:63212656 G>A maps to NM_178505.6 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr23:15657827 C>A did not map to a codon.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr23:15646094 C>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:15657879 C>G did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:15677137 C>G did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr14:61747088 C>A maps to NM_001017970.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:41956197 G>A maps to NM_018126.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr19:16791276 C>T maps to NM_024074.1 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:16791206 G>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr9:108536276 C>A maps to NM_018112.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr1:32542889 C>T maps to NM_018056.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr3:12780075 C>A maps to ENST00000431022 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:14170985 G>A maps to NM_024334.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr3:194309344 G>T maps to NM_001166305.1 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr11:129722406 A>G maps to NM_138788.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr23:34657477 G>A did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr1:15545932 G>A maps to NM_018022.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr1:15541864 C>T maps to NM_018022.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:45120239 G>A maps to NM_024587.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:33363912 C>G maps to NM_033504.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr1:25783155 T>A maps to NM_018202.4 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr1:25785215 G>A maps to NM_018202.4 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:77423414 G>C maps to NM_032936.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:226065175 C>A maps to NM_014698.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:44116029 G>A maps to NM_018426.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr14:77686393 C>A maps to NM_020431.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr8:29927356 C>A maps to NM_016127.4 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr8:94792819 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:56663693 C>A maps to ENST00000434581 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr10:45430566 C>T maps to NM_001123376.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:109796877 C>T maps to NM_153015.1 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:109796814 C>A maps to NM_153015.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:16069352 T>C maps to NM_001013641.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:18723291 T>G maps to NM_153347.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr15:42519098 C>A maps to ENST00000389834 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr16:424307 G>C maps to NM_021259.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:424043 G>A maps to NM_021259.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr16:424039 G>A maps to NM_021259.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:35853136 G>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr14:74874673 C>A maps to NM_001105579.1 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr20:24524212 G>A maps to NM_024893.1 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr20:24523789 T>C maps to NM_024893.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:41888701 C>A maps to NM_001098821.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr17:26652618 G>T maps to NM_014573.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr17:38991085 G>A maps to NM_001195386.1 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr3:69101201 G>A maps to NM_007114.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr3:69072405 T>C maps to NM_007114.2 E1068E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:46750622 G>A maps to NM_147196.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:4298100 G>T maps to NM_144615.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:154741381 A>T did not map to a codon.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr23:154774820 G>C did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr1:151146053 T>C maps to NM_013353.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr3:33135654 C>T maps to NM_001039770.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr3:33134445 G>C maps to NM_001039770.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr3:33134424 T>C maps to NM_001039770.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:69094471 A>G maps to NM_182502.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr4:69101751 C>T maps to NM_182502.3 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr4:69334595 G>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:68938143 A>G maps to NM_207407.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:117787939 C>A maps to ENST00000413475 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr21:19670049 C>A did not map to a codon.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr21:19737473 G>T maps to NM_002772.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr21:19715876 A>G maps to NM_002772.2 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr21:19744573 A>T maps to NM_002772.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr21:19715858 A>G maps to NM_002772.2 Y464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr21:19647651 A>C maps to NM_002772.2 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr21:19716353 C>A maps to NM_002772.2 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:42843868 C>T maps to NM_001135099.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr11:117969766 C>T maps to NM_019894.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr11:117978578 G>A maps to NM_019894.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:117973861 C>G maps to NM_019894.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:111768697 G>T maps to ENST00000443106 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr19:2422217 G>T maps to NM_182973.1 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:29904606 G>T maps to NM_001193451.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5241-01A-01D-1441-08 chr12:29665041 C>A maps to NM_001193451.1 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr12:29725063 C>A maps to NM_001193451.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr12:29911674 C>T maps to NM_001193451.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr12:88586607 G>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr13:101316527 C>A maps to NM_032813.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr13:101287429 C>A maps to NM_032813.2 G408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr11:57506182 T>C maps to NM_015959.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr18:66344307 T>G maps to NM_019022.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr18:66367643 A>G maps to NM_019022.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr20:7963242 A>T maps to NM_021156.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr20:7980392 G>T maps to NM_021156.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr9:117798446 T>C maps to NM_002160.2 E1862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr9:117808739 C>A maps to NM_002160.2 G1692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr9:117846752 T>C did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr9:117810680 C>G maps to NM_002160.2 L1570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr14:103599088 A>C maps to NM_006291.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr6:138196126 C>G maps to NM_006290.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr6:138192645 G>C maps to NM_006290.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:138198378 C>T maps to NM_006290.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr2:152214239 C>T maps to NM_007115.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr8:22887121 C>A did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr8:23002046 G>A maps to NM_003840.3 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr8:23003214 C>T maps to NM_003840.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr8:119938862 G>T maps to NM_002546.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:119936777 G>A maps to NM_002546.3 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr17:16843025 C>T maps to NM_012452.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr22:42322213 G>T maps to NM_052945.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr16:12061698 A>C maps to NM_001192.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr12:6440076 C>A maps to NM_001065.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr20:62329795 C>G maps to NM_003823.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:12169668 C>T maps to NM_001243.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:12175712 A>G maps to NM_001243.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr1:7995184 C>T maps to NM_001561.5 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:172224299 C>A maps to ENST00000382750 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr3:172227049 G>A maps to ENST00000382750 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:7462438 C>G maps to NM_003808.3 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:7462448 C>T maps to NM_003808.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr13:108955863 C>G maps to NM_006573.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:6669936 C>A maps to NM_003807.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:173020012 A>G maps to NM_005092.3 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:173155729 G>A maps to NM_003326.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:170802910 G>A maps to NM_015028.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr3:170811626 C>T did not map to a codon.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr3:170784431 A>G maps to NM_015028.2 Y1264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:170819283 C>A maps to NM_015028.2 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr4:2746618 G>A maps to NM_024309.3 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr4:2749603 G>C maps to NM_024309.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr4:122079901 C>A maps to ENST00000509841 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:195599178 G>A maps to NM_001010938.1 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr3:195595137 C>A maps to NM_001010938.1 G740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr3:195605215 G>A maps to NM_001010938.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr8:9605565 C>T maps to NM_003747.2 Y892Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr11:57080094 C>A maps to NM_033396.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr11:57076302 T>A maps to NM_033396.2 A1294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr11:57088088 C>A maps to NM_033396.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr10:93619219 G>T maps to NM_025235.3 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:99854653 C>G did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:99854695 C>A did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:99854604 C>A did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:175052997 C>T maps to NM_022093.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:175046646 C>A maps to NM_022093.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:175054539 G>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:175092791 C>G maps to NM_022093.1 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:175049350 G>T maps to NM_022093.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr1:175092653 C>T maps to NM_022093.1 D923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr1:175046706 C>A maps to NM_022093.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:175087721 C>A maps to NM_022093.1 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:55665558 G>A maps to ENST00000344887 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:74832985 A>G maps to NM_001112808.2 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr1:74701804 C>T maps to NM_001112808.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:55645562 A>G maps to NM_003283.4 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:201334330 G>C maps to ENST00000421663 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr11:1955617 G>A maps to ENST00000397301 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:11362726 C>T maps to NM_005425.4 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr19:12816127 C>A maps to NM_001136196.1 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr7:128640533 G>A maps to ENST00000471166 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:175375790 G>A maps to NM_003285.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr1:175325458 A>C maps to NM_003285.2 S1038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr1:175292528 G>A maps to NM_003285.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:175335251 G>T maps to NM_003285.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:175331871 G>T maps to NM_003285.2 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:175355324 C>A maps to NM_003285.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr1:175335164 G>T maps to NM_003285.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:175348686 C>A did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:175372336 T>C maps to NM_003285.2 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:175375661 C>A maps to NM_003285.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr1:175299208 C>G did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:175292495 G>A maps to NM_003285.2 F1358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr7:5352352 C>T maps to NM_001080495.2 A2723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:5391686 C>A maps to NM_001080495.2 E1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr22:40660694 C>G maps to ENST00000454349 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr22:40657836 G>A maps to ENST00000454349 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr22:40662451 C>T maps to ENST00000454349 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:218713625 G>T maps to NM_022648.4 T413T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-22-5474-01A-01D-1632-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr7:47453596 T>C did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:32063502 G>A maps to ENST00000375244 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:32020576 C>T maps to ENST00000375244 V2995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr6:32016320 G>T maps to ENST00000375244 P3288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:32017775 C>G maps to ENST00000375244 T3146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:32023669 C>A maps to ENST00000375244 E2809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr6:32047065 C>A maps to ENST00000375244 P1373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr6:32036725 G>C maps to ENST00000375244 V1925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr22:35723367 G>T maps to ENST00000451197 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr17:52993165 C>T maps to NM_005486.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr17:52978258 C>G maps to NM_005486.2 Y11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr1:235291985 G>A maps to NM_014765.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr14:58869445 G>T maps to NM_207377.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr20:43585126 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:45396131 C>A maps to NM_006114.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr3:100105170 C>T maps to NM_014820.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:144406792 C>T maps to NM_052963.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:144407559 C>T maps to NM_052963.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr8:144406774 C>A maps to NM_052963.1 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:25686808 T>C maps to ENST00000264331 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr3:25686853 T>G maps to ENST00000264331 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:18194299 G>A maps to NM_004618.3 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr17:18212201 A>C maps to NM_004618.3 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr17:18210213 T>A maps to NM_004618.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:22322061 G>A maps to NM_003935.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr22:22322089 T>C did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:133327498 T>A maps to NM_007027.3 T1435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:133335769 C>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:32543157 C>A maps to NM_005802.4 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr1:179815247 G>C maps to NM_145034.4 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:132566463 C>A maps to NM_014506.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr8:59852026 G>T maps to NM_014729.2 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr8:59720306 C>T maps to NM_014729.2 *527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr8:59728235 C>G maps to NM_014729.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr20:42694503 C>T maps to ENST00000348077 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr20:42683147 G>T maps to ENST00000348077 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:52473847 G>A maps to ENST00000407228 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:52480034 C>A maps to ENST00000407228 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr17:7577608 C>A did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr17:7579479 A>G maps to NM_001126112.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:7577024 T>A maps to NM_001126112.1 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr17:7579493 T>A maps to NM_001126112.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr17:7579484 C>A maps to NM_001126112.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr17:7577126 C>A maps to NM_001126112.1 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr17:7576927 T>A did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:7579377 G>T maps to NM_001126112.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr17:7576850 A>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr17:7577155 C>A did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:7577078 C>A maps to NM_001126112.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr17:7574034 T>C did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr15:43707871 G>C maps to NM_001141980.1 S1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr15:43762213 G>A maps to NM_001141980.1 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:43712599 G>T maps to NM_001141980.1 Y1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:223989848 G>A maps to NM_001031685.2 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr20:44004179 G>A maps to NM_014477.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr3:189526203 C>T maps to NM_003722.4 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr6:83075379 C>T maps to NM_006670.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr6:83075248 C>T maps to NM_006670.4 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr11:68851474 G>A maps to NM_139075.3 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr11:68838834 C>T maps to NM_139075.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:68855387 G>A maps to NM_139075.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr20:62505155 C>T maps to NM_199360.1 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr9:6328675 C>T maps to NM_033516.5 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:6328992 C>G maps to NM_033516.5 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr11:18051057 C>T did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr12:72372759 G>A maps to ENST00000389376 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr12:72335392 C>T maps to ENST00000389376 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:6976807 C>T maps to NM_001159287.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr15:63356323 C>G maps to ENST00000380364 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr9:35685690 G>C maps to ENST00000329305 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:154145417 C>A maps to NM_001043351.1 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:1491689 T>C maps to NM_000547.5 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr13:103326656 C>T maps to ENST00000376052 T1132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr13:103296992 G>T maps to ENST00000376052 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:186300713 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:186324871 T>C maps to NM_003292.2 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr1:186308814 T>C maps to NM_003292.2 Q1370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:186326587 C>A maps to NM_003292.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:186303598 T>C maps to NM_003292.2 K1680K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr1:186330007 C>A maps to NM_003292.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:188933166 G>A maps to NM_198485.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr3:188956623 G>T maps to NM_198485.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr1:3544177 G>T maps to NM_182752.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr9:140093945 G>T maps to NM_001128228.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr21:10942774 C>A did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr21:10906915 C>A maps to NM_199261.2 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr21:10943021 T>C did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr21:10920106 G>A maps to NM_199261.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr21:10908859 G>A maps to NM_199261.2 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr21:10971317 G>C maps to NM_199261.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr21:10908866 G>T maps to NM_199261.2 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr13:20025323 A>G maps to NM_199254.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr13:20012294 T>C did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr13:20039416 G>A maps to NM_199254.2 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr16:67189188 C>T maps to NM_003789.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr16:67188722 G>A maps to NM_003789.3 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:123675836 C>A maps to NM_001190945.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr9:123675886 C>A maps to NM_001190945.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr9:139802568 G>T maps to ENST00000359662 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr14:103336546 G>T maps to NM_145725.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr14:103371854 G>T maps to NM_145725.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:239261530 G>A maps to NM_015650.3 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr6:111901416 C>A maps to ENST00000340026 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr6:111887688 G>A maps to ENST00000340026 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:209935984 G>A maps to NM_025228.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:209933635 C>A maps to NM_025228.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr1:209936904 G>A maps to NM_025228.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:209948943 C>A maps to NM_025228.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:27076390 C>T maps to NM_004295.3 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:211533357 T>A maps to ENST00000427925 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:2223817 G>A maps to NM_032271.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr3:42133050 T>A maps to NM_001042646.1 C30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr4:118005531 T>A maps to NM_152402.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:52370923 G>A maps to NM_012288.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:36872546 C>A maps to NM_014831.2 E2799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr3:36872685 C>T maps to NM_014831.2 E2752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr3:36898725 G>A maps to NM_014831.2 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:36898647 G>A maps to NM_014831.2 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:36872687 C>A maps to NM_014831.2 E2752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:7834840 C>T maps to NM_001166621.1 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr16:88923572 C>T maps to NM_016209.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:7747618 C>T maps to NM_001042461.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr3:108568088 C>G maps to NM_016388.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr3:108572721 T>C maps to NM_016388.2 *187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr6:123588861 A>G maps to NM_006073.2 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr6:123600199 C>G did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr6:123600210 A>T maps to NM_006073.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr6:123687318 G>A maps to NM_006073.2 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr6:123892206 C>T maps to NM_006073.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:118530457 C>A maps to ENST00000264029 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:41250460 C>T maps to NM_018643.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr6:41243863 T>A maps to NM_018643.2 *235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr6:42227437 C>A maps to NM_033502.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:152710222 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:129695764 A>G maps to NM_007117.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr3:129695812 C>A maps to NM_007117.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr12:73015516 C>A maps to NM_013381.2 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr8:110131290 G>T maps to NM_003301.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr8:110100166 C>A maps to NM_003301.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr8:110100361 T>A maps to NM_003301.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr8:110131548 C>G maps to NM_003301.4 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:126445614 G>T maps to NM_025195.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr2:12863630 G>T maps to NM_021643.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr20:368923 A>T maps to ENST00000422053 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:30122114 G>A maps to NM_006778.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr1:228584677 C>A maps to NM_145214.2 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:18638307 C>T maps to NM_001037330.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr17:18638550 T>C maps to NM_001037330.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr11:4407426 G>A maps to NM_003141.3 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:138258361 A>G maps to NM_015905.2 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr7:138252233 T>A maps to NM_015905.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr19:59061389 C>T maps to NM_005762.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:6477539 G>A maps to NM_033278.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr9:119460297 G>T maps to NM_012210.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:114949568 A>C maps to NM_015906.3 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr1:114970453 G>A maps to NM_015906.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:114970444 C>T maps to NM_015906.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:27151767 G>A maps to NM_171982.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr17:57126640 T>C maps to NM_015294.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr6:25967058 C>T maps to NM_006355.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr6:25983830 G>T maps to NM_006355.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:30309597 A>T maps to NM_021253.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:99489825 A>T maps to NM_033017.3 L488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:30105077 C>T maps to ENST00000376724 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr3:140407245 C>A maps to NM_152616.4 Y574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:140401981 C>G maps to NM_152616.4 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:140397112 G>A maps to NM_152616.4 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:140406741 G>A maps to NM_152616.4 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr3:140401372 C>T maps to NM_152616.4 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr17:73870923 G>A maps to NM_033452.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr11:55032732 T>A maps to ENST00000357530 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr11:89531504 C>T maps to NM_020358.2 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr11:5701329 C>T maps to NM_033034.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr11:5686452 T>C maps to NM_033034.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr11:5686039 C>G maps to NM_033034.2 *494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:67047380 G>A maps to NM_184085.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr8:67064772 G>T maps to NM_184085.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr8:67047299 C>T maps to NM_184085.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr8:67040549 G>A maps to NM_184085.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:248031144 A>T did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr1:248028111 G>T maps to NM_015431.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:248031300 C>T maps to NM_015431.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:248039500 G>T maps to NM_015431.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr3:160155864 T>C maps to NM_173084.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr4:165961610 C>T maps to NM_152620.2 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:165962381 G>A maps to NM_152620.2 W386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:231337115 C>T maps to NM_001004342.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:231349680 C>T maps to NM_001004342.3 D748D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:4621769 C>T maps to NM_018073.5 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:45052026 C>T maps to NM_182985.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr15:45059594 A>T maps to NM_182985.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:31235550 G>T maps to NM_001008274.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr16:31226445 C>G maps to NM_001008274.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:75034321 C>T maps to ENST00000430211 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr14:51446262 C>A maps to ENST00000338969 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:189068015 C>G maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr4:189065246 C>A maps to NM_178556.3 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr4:189013003 A>G maps to ENST00000326754 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:189020206 G>A maps to ENST00000326754 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr4:189012670 G>T maps to ENST00000326754 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr4:189020232 C>A maps to ENST00000326754 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:14286982 G>A maps to NM_007118.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:14498736 C>T maps to NM_007118.2 L2774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr5:14389423 C>A maps to NM_007118.2 G1325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr5:14331005 A>G maps to NM_007118.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:14465676 C>T maps to NM_007118.2 R1897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr22:38120491 C>A maps to NM_001039141.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr14:92471523 A>T maps to NM_004239.3 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:92471637 T>C maps to NM_004239.3 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr14:92488130 A>G maps to NM_004239.3 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:230638890 T>A maps to ENST00000389044 P1845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr7:100466331 G>T maps to NM_003302.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:13216200 C>A maps to NM_001136035.2 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:126329536 G>T did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr22:20102129 C>G maps to ENST00000439169 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr22:20100674 G>A maps to ENST00000439169 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:100273995 C>T did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:100265656 G>C did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:100297168 G>A did not map to a codon.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr2:29093053 C>T maps to NM_017910.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:29092699 C>T maps to NM_017910.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr22:46749685 C>A maps to NM_018006.4 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:54956997 G>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:54952921 G>C did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:54948715 C>G did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr23:54955359 G>A did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:54954174 C>T did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:54957140 C>A did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:54950181 G>A did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:54952895 T>A did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:54957227 C>T did not map to a codon.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr23:54949442 G>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:54955415 T>C did not map to a codon.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr12:49725030 G>A maps to NM_005480.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:193051314 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:193038213 A>T maps to NM_004600.5 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:72935238 G>A maps to NM_007332.2 Q1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:72948635 C>G maps to NM_007332.2 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr8:72958747 G>A maps to NM_007332.2 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:72970051 C>A did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr8:72942186 G>A maps to NM_007332.2 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:72958828 G>A maps to NM_007332.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr8:72964928 A>T maps to NM_007332.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:72963054 A>T maps to NM_007332.2 C621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr8:72958839 C>A maps to NM_007332.2 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:142499868 G>T maps to ENST00000476941 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:38211569 G>A maps to NM_003306.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr20:33596468 G>A maps to NM_015638.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr20:33591290 G>C maps to NM_015638.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:111155914 G>A did not map to a codon.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr23:111025217 C>G did not map to a codon.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr23:111095582 A>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:111195428 G>C did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr23:111155953 G>T did not map to a codon.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr23:111078160 A>G did not map to a codon.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr23:111024416 G>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:111195609 C>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:111195572 C>T did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr23:111020094 C>G did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:111025339 A>G did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:111025198 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:111195318 G>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:111195370 C>G did not map to a codon.
Sequencing variant TCGA-70-6723-01A-11D-1817-08 chr23:111195614 A>T did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr11:101359754 T>A maps to NM_004621.5 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr11:101362387 C>A maps to NM_004621.5 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:135692781 C>T maps to NM_020389.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr5:135692754 C>A maps to NM_020389.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr5:135651308 G>T maps to NM_020389.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr15:31329970 G>T maps to NM_002420.4 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr15:31334347 C>T maps to NM_002420.4 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:31354781 G>T maps to NM_002420.4 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr21:45821776 G>A maps to ENST00000397932 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr21:45811238 C>T maps to ENST00000397932 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr21:45833790 G>T maps to ENST00000397932 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr21:45821653 C>A maps to ENST00000397932 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr21:45815336 C>G maps to ENST00000397932 S612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr9:73213400 G>A maps to ENST00000419692 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr9:73736161 G>T maps to NM_001007471.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr9:73151042 G>T maps to ENST00000419692 T1616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr9:73213484 G>C maps to ENST00000419692 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr9:73296449 A>G maps to ENST00000419692 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:73478021 G>A maps to ENST00000419692 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr9:73236183 T>C maps to ENST00000419692 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr9:73233932 C>G maps to ENST00000419692 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr9:73151519 C>G maps to ENST00000419692 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr19:49692231 G>T maps to NM_017636.3 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:2434713 G>A maps to ENST00000452833 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr11:2435350 G>T maps to ENST00000452833 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr9:77377802 G>A maps to NM_017662.4 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:77455048 G>T maps to NM_017662.4 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:234835253 G>T maps to NM_024080.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:234869589 C>T maps to NM_024080.4 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:116426592 G>A maps to NM_014112.2 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:116616833 G>A maps to NM_014112.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr8:116617105 C>A maps to NM_014112.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:116616593 C>A maps to NM_014112.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:3427650 G>A maps to ENST00000381913 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:110252355 G>A maps to NM_021625.4 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr7:142605793 C>T maps to NM_019841.4 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr7:142612554 T>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr7:98519470 G>A maps to ENST00000359863 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr7:98546247 A>G maps to ENST00000359863 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr7:98508831 G>T maps to ENST00000359863 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr7:98608730 C>G maps to ENST00000359863 L3651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr7:98601939 C>A maps to ENST00000359863 C3465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:98601959 C>A maps to ENST00000359863 S3472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr9:131084582 C>G maps to NM_015679.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:135778002 G>A maps to NM_000368.4 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:135796753 G>T maps to NM_000368.4 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr16:2129555 A>T did not map to a codon.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr16:2129609 G>T maps to NM_000548.3 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr16:2106195 G>T did not map to a codon.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr3:150128693 T>A maps to NM_014779.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:107018451 G>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr3:12531400 G>T maps to NM_025265.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:54695430 G>A maps to NM_001077446.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:54696027 C>A maps to NM_001077446.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr17:73517589 C>A maps to NM_207346.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr17:73512833 G>T maps to NM_207346.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr17:73517537 G>T maps to NM_207346.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:18503268 G>A maps to NM_006292.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr11:18536389 T>G did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:99635066 A>G maps to NM_025244.2 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr2:99634802 G>A maps to NM_025244.2 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr11:65721059 C>A maps to NM_152762.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:81609985 C>A maps to NM_000369.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:81528490 G>T did not map to a codon.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr18:72999993 G>T maps to NM_005786.4 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr18:73000058 C>A maps to NM_005786.4 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr20:51872342 T>C maps to NM_173485.5 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr20:51872315 G>A maps to NM_173485.5 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr20:51870995 C>T maps to NM_173485.5 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:31768607 G>A maps to NM_020856.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:31768907 G>A maps to NM_020856.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:31768044 G>T maps to NM_020856.2 S885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:31770266 C>T maps to NM_020856.2 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr19:50247495 G>C maps to NM_021733.1 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:76506860 C>T maps to NM_015516.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:110407608 A>G maps to NM_033035.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr2:122522918 G>A maps to NM_004622.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr8:143412281 C>T maps to ENST00000445818 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr12:31135495 C>T maps to NM_001080509.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr10:71243547 C>T maps to NM_012339.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr12:58140911 G>T maps to NM_005981.3 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:2337819 C>G maps to NM_139022.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:128802732 C>T maps to NM_178562.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr7:128807654 C>T maps to NM_178562.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr7:128802337 C>A maps to NM_178562.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr4:99407999 G>T maps to NM_005723.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:38546899 C>A did not map to a codon.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr23:38546887 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr24:9305959 C>A did not map to a codon.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr24:9305916 A>G did not map to a codon.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr24:6115609 A>G did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr24:6115632 T>C did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr24:6114378 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:53117070 C>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:3200789 T>A did not map to a codon.
Multiple mappings detected for codon TCGA-18-5592-01A-01D-1632-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-43-6770-01A-11D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr6:43230655 G>A maps to NM_032538.1 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:43220490 G>T maps to NM_032538.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr6:43250734 G>T maps to NM_032538.1 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr11:113235650 C>T maps to NM_017868.3 N637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr11:113222835 C>T maps to NM_017868.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:231069607 C>A did not map to a codon.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr1:231047277 G>A maps to NM_024525.4 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:180320738 G>T maps to NM_133462.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr3:180328229 C>G maps to NM_133462.3 S738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr3:180328167 T>C maps to NM_133462.3 N717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr10:75113470 G>A maps to NM_145170.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr10:75056898 G>T maps to NM_145170.3 Y585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr10:75113479 A>G maps to NM_145170.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:166771832 C>A maps to NM_024753.3 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:166786170 C>A maps to NM_024753.3 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr5:34850334 C>A maps to NM_144725.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr17:40113407 C>T maps to ENST00000377543 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr7:138822648 T>C maps to NM_024926.2 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:32855588 G>T did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr2:32855588 G>T did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr2:32865347 G>T maps to NM_017735.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr21:38512874 C>T maps to NM_003316.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr21:38459619 T>A maps to NM_003316.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr21:38573769 C>T maps to NM_003316.3 S1991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:178481725 G>A maps to NM_152275.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr2:178482679 C>A maps to NM_152275.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:178415698 G>C maps to NM_152517.2 S598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr5:40716429 T>C maps to NM_012382.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:109462666 A>T maps to NM_014673.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr11:118398236 C>T maps to NM_001080441.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr5:94852863 G>C maps to NM_014639.3 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr14:91252595 G>A maps to NM_001010854.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr14:91059950 C>A maps to NM_001010854.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr14:89337997 T>C maps to NM_144596.2 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:117629134 C>T maps to NM_003594.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:113258795 C>G maps to NM_153712.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr22:43564145 C>T maps to NM_015140.3 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:167752258 C>T maps to NM_031949.4 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:167753789 A>G maps to NM_031949.4 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:9874873 G>A maps to NM_001025930.3 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:9877136 G>A maps to NM_001025930.3 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:219617858 G>A maps to NM_014640.4 W1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:219602935 A>C maps to NM_014640.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr14:76232417 A>G maps to NM_015072.4 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr14:76286426 C>T maps to NM_015072.4 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:76219244 C>A maps to NM_015072.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:46868811 G>C maps to NM_001130918.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr1:84399337 C>A maps to NM_024686.4 G334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr1:84417876 T>C maps to NM_024686.4 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr1:84372074 G>A maps to NM_024686.4 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:50470357 G>T maps to NM_001080447.1 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179407952 C>T maps to NM_133378.4 W29681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179429954 G>A maps to NM_133378.4 I24400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179430569 A>G maps to NM_133378.4 F24195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179431328 T>C maps to NM_133378.4 K23942K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179438045 T>C maps to NM_133378.4 K21703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179463550 C>T maps to NM_133378.4 R16394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179594457 C>T maps to NM_133378.4 G4930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179621105 C>T maps to NM_133437.3 K3528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179640776 G>A maps to NM_133378.4 V1938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:179648862 C>T maps to NM_133378.4 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr2:179434028 G>T maps to NM_133378.4 V23042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr2:179593230 C>T maps to NM_133378.4 V5230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:179479400 G>T maps to NM_133378.4 A13712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:179397112 A>G maps to NM_133378.4 Y32175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:179582844 A>T maps to NM_133378.4 S7052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:179583558 G>T maps to NM_133378.4 S6879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr2:179597011 G>A maps to NM_133378.4 Q4318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr2:179604795 T>A maps to NM_133437.3 P4217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr2:179590614 T>A maps to NM_133378.4 K5568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr2:179632623 G>C maps to NM_133378.4 V3111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr2:179644750 C>A maps to NM_133378.4 V1235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:179613059 C>T maps to ENST00000375038 E4691E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr2:179640548 G>T maps to NM_133378.4 T2014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr2:179408665 A>G maps to NM_133378.4 L29501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr2:179611916 T>C maps to ENST00000375038 L5072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:179474027 G>A maps to NM_133378.4 R14769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:179497444 C>A maps to NM_133378.4 E11862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:179590305 T>C maps to NM_133378.4 A5631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr2:179585309 C>A maps to NM_133378.4 G6483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:179431322 G>A maps to NM_133378.4 I23944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:179605623 C>T maps to NM_133437.3 Q3941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr2:179579025 G>A maps to NM_133378.4 S7581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr2:179605170 C>T maps to NM_133437.3 L4092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:179422804 A>G maps to NM_133378.4 N26524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr2:179455977 A>T maps to NM_133378.4 G17590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr2:179569456 A>G maps to NM_133378.4 D8670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:179628931 G>T maps to NM_133378.4 A3362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:179635940 C>A maps to NM_133378.4 E2705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr2:179402306 A>G maps to NM_133378.4 A30641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:179544137 C>A maps to NM_133378.4 E9980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:179395576 A>C maps to NM_133378.4 S32687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:179602983 C>T maps to NM_133378.4 Q3488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr2:179644759 A>G maps to NM_133378.4 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:179437166 T>C maps to NM_133378.4 K21996K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:179644906 G>C maps to NM_133378.4 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr2:179644882 T>C maps to NM_133378.4 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:179400808 G>T maps to NM_133378.4 L30987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr2:179414545 C>A maps to NM_133378.4 E28067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:179404839 C>A maps to NM_133378.4 E30117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:179464428 G>C maps to NM_133378.4 L16165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:179500825 G>T maps to NM_133378.4 G11256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:179605785 C>T maps to NM_133437.3 K3887K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-34-5231-01A-21D-1817-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr2:179576076 C>T did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr2:179586756 G>A maps to NM_133378.4 R6301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr2:179442157 G>T maps to NM_133378.4 A20400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:179614215 G>C maps to ENST00000375038 S4306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:179464029 C>T maps to NM_133378.4 K16262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr2:179486013 G>C maps to NM_133378.4 S12576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr2:179597600 G>T maps to NM_133378.4 S4190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr2:179456220 G>C maps to NM_133378.4 S17509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:179499895 G>T maps to NM_133378.4 S11439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:179642225 G>A maps to NM_133378.4 P1522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5029-01A-01D-1441-08 chr2:179648820 T>C maps to NM_133378.4 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr2:179506970 C>G maps to NM_133378.4 L10949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr2:179431457 A>G maps to NM_133378.4 A23899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr2:179393644 T>C maps to NM_133378.4 A33043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr2:179516471 G>T maps to NM_133378.4 T10694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:179588004 T>A maps to NM_133378.4 P5999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:179613191 A>G maps to ENST00000375038 Y4647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr2:179611813 G>A maps to ENST00000375038 R5107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:179407937 G>T maps to NM_133378.4 T29686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:179416981 G>T maps to NM_133378.4 V27647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr2:179438953 C>A maps to NM_133378.4 G21401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:179455491 G>T maps to NM_133378.4 V17752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:179460332 G>A maps to NM_133378.4 Q16682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr2:179550281 G>A maps to NM_133378.4 H9541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr2:179581921 C>A maps to NM_133378.4 L7269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr2:179579803 C>A maps to NM_133378.4 L7459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr2:179596202 G>A maps to NM_133378.4 L4520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr2:179546412 T>G maps to NM_133378.4 T9805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr2:179399113 C>T maps to NM_133378.4 K31508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr2:179633589 T>A maps to NM_133378.4 T2991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr2:179584770 A>G maps to NM_133378.4 Y6622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr2:179499516 C>G maps to NM_133378.4 L11460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:179437985 A>G maps to NM_133378.4 H21723H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr2:179457259 G>A maps to NM_133378.4 D17256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:179458089 C>A maps to NM_133378.4 L17047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr2:179572472 C>T maps to NM_133378.4 V8363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr2:179596698 C>A did not map to a codon.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr2:179610752 A>G maps to ENST00000375038 C5460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:179447925 A>G maps to NM_133378.4 A19300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr2:179621083 T>A maps to NM_133437.3 K3536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:179441932 G>A maps to NM_133378.4 P20475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:179453426 G>A maps to NM_133378.4 R18441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:179631291 G>A maps to NM_133378.4 D3173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:179649051 G>T maps to NM_133378.4 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:179659272 T>C maps to NM_133378.4 K417K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:179604276 G>C maps to NM_133437.3 V4390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr2:179571595 G>A maps to NM_133378.4 V8465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:179438156 A>T maps to NM_133378.4 I21666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:179515496 C>G maps to NM_133378.4 A10796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:179616707 T>C maps to ENST00000375038 S3475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr2:179633505 T>C maps to NM_133378.4 K3019K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:179396749 C>T maps to NM_133378.4 P32296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:179664419 T>A maps to NM_133378.4 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:179544671 C>A maps to NM_133378.4 E9933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr2:179421740 G>A maps to NM_133378.4 G26812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr2:179409129 T>A maps to NM_133378.4 V29374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr2:179664350 C>A maps to NM_133378.4 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:179412488 C>T maps to NM_133378.4 L28720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr2:179426189 C>G maps to NM_133378.4 L25655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:179553855 A>T maps to NM_133378.4 A9429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:179425814 A>T maps to NM_133378.4 V25780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:179437673 A>G maps to NM_133378.4 Y21827Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:179556763 C>A maps to NM_133378.4 E9337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:179588730 G>T maps to NM_133378.4 V5841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:179582535 C>T maps to NM_133378.4 A7111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:179591832 G>T maps to NM_133378.4 T5509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:179604758 G>T maps to NM_133437.3 R4230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr2:179643973 A>T maps to NM_133378.4 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:179432906 A>T maps to NM_133378.4 A23416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:179545845 G>T maps to NM_133378.4 T9856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr20:43113109 T>C maps to NM_024331.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:72245531 C>T maps to NM_032646.5 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr17:72218787 C>T maps to NM_032646.5 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr17:72245211 C>T maps to NM_032646.5 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr17:72239530 G>T maps to NM_032646.5 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr7:2692644 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:49666169 C>A maps to NM_032704.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr12:49666850 G>A maps to NM_032704.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr12:49666041 C>T maps to NM_032704.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr13:19753679 C>A maps to NM_006001.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:132237811 G>T maps to NM_080386.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:130953818 A>G maps to NM_207312.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr2:220115570 C>A maps to NM_006000.1 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:220115076 T>C maps to NM_006000.1 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr22:18609317 C>A maps to NM_018943.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:30691667 G>T maps to NM_178014.2 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr16:90001434 G>T maps to ENST00000304984 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr4:190905410 G>T maps to ENST00000248151 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr18:12325636 C>A maps to NM_032525.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr17:57951924 G>A maps to NM_016261.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr17:57937724 G>A maps to NM_016261.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr17:57955527 C>T maps to NM_016261.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:135099072 G>A maps to NM_006659.2 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr10:135106681 G>T maps to NM_006659.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr10:135106043 C>G maps to NM_006659.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:135102435 C>G maps to NM_006659.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr10:135106714 C>T maps to NM_006659.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr10:135095750 C>A maps to NM_006659.2 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:113212712 A>G maps to NM_006322.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr13:113158972 G>A maps to NM_006322.4 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr15:43690254 A>G maps to ENST00000399460 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr15:22861914 G>C maps to NM_052903.4 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:22867507 G>T maps to NM_052903.4 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:22853810 G>T maps to NM_052903.4 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr15:22840317 G>A maps to NM_052903.4 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr22:50662624 G>A maps to NM_020461.3 R739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr22:50682675 G>C maps to NM_020461.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr22:50678787 C>A maps to NM_020461.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr22:50665439 G>A maps to NM_020461.3 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr16:28856349 G>A maps to NM_003321.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:49391431 G>A maps to NM_003323.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr12:3039412 G>C did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr6:158924187 C>T maps to NM_020245.3 R1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr8:15508304 G>T maps to NM_006765.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr11:62342866 C>T maps to NM_022830.2 W813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr3:52263187 C>A maps to NM_007284.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr7:19738154 C>G maps to NM_001002926.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr1:32657925 C>G maps to NM_175852.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:16846271 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:16858000 G>T did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:16836852 G>C did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr16:11785815 T>C maps to ENST00000356957 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr16:11785785 C>A maps to ENST00000356957 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:134223871 G>A maps to NM_024715.3 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:52936764 G>T maps to NM_020784.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr18:9886976 C>A maps to NM_001098529.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr7:37907338 T>C maps to NM_016616.4 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr3:138025269 G>T maps to ENST00000333911 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr12:104721445 C>G maps to NM_001093771.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:19903293 C>T maps to NM_006440.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr22:19885648 C>A maps to NM_006440.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr22:19865932 C>A maps to NM_006440.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr22:19864683 G>A maps to NM_006440.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:10477139 G>T maps to NM_003331.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:10465285 C>G did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr11:89017959 C>T maps to NM_000372.4 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:88911286 C>T maps to NM_000372.4 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr15:41862285 G>A maps to NM_006293.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr15:41862507 C>A maps to NM_006293.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr15:41862297 G>A maps to NM_006293.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:36398482 C>T did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr9:12695713 A>C maps to NM_000550.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:71899757 C>G maps to NM_173555.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr7:66490006 A>T maps to NM_018264.2 K328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr7:66548449 G>A maps to NM_018264.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr19:56180886 G>C maps to NM_007279.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr15:70960256 G>A maps to NM_018003.2 Y922Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:70976769 T>A maps to NM_018003.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr15:70961108 T>C maps to NM_018003.2 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr23:47070250 C>T did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:47070572 G>C did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:47072254 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:69112185 G>A maps to NM_003968.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr4:68527923 C>A maps to NM_018227.5 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:49848861 C>T maps to NM_003335.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:49847488 T>A maps to NM_003335.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:34241646 G>C maps to NM_001171201.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr9:33927888 G>C maps to NM_018449.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:33948492 C>A maps to NM_018449.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:154229594 C>T maps to NM_014847.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr1:154221797 C>T maps to NM_014847.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr11:122669742 G>A did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr11:122650302 T>A maps to NM_032873.4 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr11:122653770 G>T maps to NM_032873.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:122678808 C>A maps to NM_032873.4 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr11:122653833 C>A maps to NM_032873.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr17:16285541 G>A maps to NM_018955.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr12:125397879 C>A maps to NM_021009.5 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:118717207 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:118708715 G>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr20:44444262 G>A maps to NM_007019.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:83748180 T>C maps to NM_198920.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:83754350 C>A maps to NM_198920.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:23541126 G>T maps to NM_152653.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:181927581 A>T maps to NM_182678.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:4192628 C>A maps to NM_003342.4 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr11:57319959 C>A maps to NM_004223.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr12:93804844 A>G maps to NM_003348.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr23:142967237 C>A did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:142967582 G>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:142967472 A>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:142967586 C>G did not map to a codon.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr23:142967550 A>C did not map to a codon.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr23:142967582 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:74387584 G>A maps to NM_022066.3 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr17:74394576 C>A maps to NM_022066.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:55912920 G>T maps to NM_014501.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr1:202302222 T>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr15:25616126 G>A maps to NM_000462.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr15:25616071 T>A maps to NM_000462.2 K420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr12:109962290 G>T maps to NM_183415.1 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr12:109971308 C>T maps to NM_183415.1 F987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr7:156967696 C>T maps to NM_014671.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:156974311 G>A maps to NM_014671.2 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr7:157013450 G>T maps to NM_014671.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:118235858 C>T maps to NM_004788.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr11:118247310 G>A maps to NM_004788.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:153713987 C>A did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr15:74738471 G>A maps to NM_201265.1 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr15:74751085 T>A maps to NM_201265.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr16:4924933 C>A maps to NM_016936.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:138946237 C>T maps to NM_173569.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:56591545 C>T did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:56590723 A>T did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:56591636 C>T did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr11:5530344 A>G maps to NM_017481.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:156020105 G>C maps to NM_020131.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:5536291 C>T maps to NM_145053.4 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:5537008 G>A maps to NM_145053.4 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr11:5537173 C>A maps to NM_145053.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr15:43363017 C>A maps to NM_174916.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr15:43313513 G>A maps to NM_174916.2 Q967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr15:43363117 T>A maps to NM_174916.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr15:43281053 C>A maps to NM_174916.2 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr6:42631064 T>C maps to NM_015255.2 D1202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr6:42603238 A>G maps to NM_015255.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:170936430 C>T maps to ENST00000442603 C1798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr1:19447773 G>A maps to ENST00000375267 A3350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr1:19491315 G>T maps to ENST00000375267 T1496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr1:19501465 C>T maps to ENST00000375267 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr1:19467976 A>G maps to ENST00000375267 N2784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:103312246 G>A maps to NM_015902.4 D1029D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr8:103274249 A>G maps to NM_015902.4 L2579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr8:103340025 A>T maps to NM_015902.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:93676180 G>A maps to NM_175748.3 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr14:93677054 G>C did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr14:93686749 C>G maps to NM_175748.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr14:93685053 C>T maps to NM_175748.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr10:99330048 G>A maps to NM_024954.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr17:42289029 G>A maps to NM_014233.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:42289009 C>T maps to NM_014233.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:42289032 G>A maps to NM_014233.2 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:20517188 G>T maps to NM_152376.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:26608935 G>A maps to NM_183008.2 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:26611996 G>C maps to NM_183008.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr2:136519469 C>T maps to NM_014607.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:4446552 C>A maps to NM_025241.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:4447573 C>T maps to NM_025241.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr3:196083657 G>T maps to NM_015562.1 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr8:30623804 C>A maps to ENST00000265616 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:192998515 A>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr1:193018981 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:192993076 C>A did not map to a codon.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:62571823 C>T maps to NM_017859.3 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr11:18566212 T>A maps to NM_001040697.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr13:38934881 G>A maps to NM_016617.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr4:186343690 G>C maps to NM_018359.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr2:128922351 A>G maps to NM_020120.3 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr2:128878863 C>A maps to NM_020120.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr13:96555253 C>A maps to NM_020121.3 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr13:96513121 C>T maps to NM_020121.3 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr2:64112850 T>A maps to NM_006759.3 L235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr2:64109730 G>A maps to NM_006759.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:234545254 G>C maps to NM_019075.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:234622110 G>A maps to NM_019078.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:70462037 G>T maps to NM_006798.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr4:70512822 T>C maps to ENST00000514019 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr4:69795617 C>G maps to NM_024743.3 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr4:69796921 T>C maps to NM_024743.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr4:69512833 C>T maps to NM_001076.2 K527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:70160365 C>T maps to NM_053039.1 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr4:70156508 G>A maps to NM_053039.1 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr4:70146439 C>A maps to NM_053039.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr4:70352342 G>T maps to NM_021139.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr4:70361030 A>G maps to NM_021139.2 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr4:70351092 A>G maps to NM_021139.2 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr5:35966003 G>A maps to NM_152404.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:35954498 G>A maps to NM_152404.3 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr5:36049407 C>T maps to NM_174914.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:36037941 C>A maps to NM_174914.3 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr4:115589239 G>A did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr6:34835143 C>T maps to NM_017754.3 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:34826574 A>G maps to NM_017754.3 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:100453797 G>A maps to NM_015054.1 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr9:6460734 C>A maps to NM_152896.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr6:150291167 C>T maps to NM_025218.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr12:132404131 C>T maps to NM_003565.2 Q934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr16:20357447 C>T maps to ENST00000424589 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr21:43547286 G>T maps to NM_173568.3 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr21:43522279 C>T maps to NM_173568.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr21:43510516 G>T maps to NM_173568.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:124458953 G>T maps to NM_000373.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:17728601 C>T maps to ENST00000428389 P1577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:17743601 A>T maps to ENST00000428389 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr19:17738670 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:54630614 G>A maps to ENST00000260323 R1547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:54914534 C>T maps to ENST00000260323 S2039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr15:54586200 G>T maps to ENST00000260323 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr15:54305471 G>A maps to ENST00000260323 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr15:54707197 C>T maps to ENST00000260323 N1622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr15:54305589 G>T maps to ENST00000260323 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr15:54586234 G>T maps to ENST00000260323 G1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr15:54825264 G>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr15:54793156 T>A maps to ENST00000260323 L1761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr15:54799354 C>G maps to ENST00000260323 S1781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr15:54707215 C>T maps to ENST00000260323 A1628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr15:54592472 G>C maps to ENST00000260323 G1390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr15:54307001 G>C maps to ENST00000260323 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:54306923 A>C maps to ENST00000260323 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr15:54630611 A>T maps to ENST00000260323 V1546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr17:73827392 C>T maps to ENST00000412096 V828V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr15:91489918 A>T maps to NM_018671.3 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr17:33491077 T>A maps to NM_173167.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:33498365 C>A maps to NM_173167.2 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr17:33501266 A>T maps to NM_173167.2 K615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr10:73047493 G>A maps to NM_170744.3 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:96140177 G>A maps to NM_003728.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:96163713 C>T maps to NM_003728.3 W325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr4:96222806 C>T maps to NM_003728.3 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr4:96163622 G>T maps to NM_003728.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr4:96140438 G>T maps to NM_003728.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:96222889 G>T maps to NM_003728.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr6:41002665 C>A maps to NM_173561.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:35406912 C>T maps to ENST00000416672 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr8:35406924 C>G maps to ENST00000416672 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:35579872 A>T maps to ENST00000416672 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr8:35583955 C>A maps to ENST00000416672 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr8:35541201 C>T maps to ENST00000416672 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr8:35648047 C>T maps to ENST00000416672 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr8:35544207 A>G maps to ENST00000416672 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr6:167717470 G>T maps to NM_018974.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:167728873 G>A maps to NM_018974.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr6:167728849 G>T maps to NM_018974.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr7:1273219 C>A maps to NM_001080461.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr16:1417164 G>A maps to ENST00000508903 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:18961003 C>T maps to ENST00000418384 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr10:12077310 T>A maps to NM_015542.2 K38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr10:12071425 G>A maps to NM_015542.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr10:11997497 T>C maps to NM_015542.2 Q861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:118979256 G>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:118986804 G>C did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:118986835 G>A did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:118985784 G>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:118972474 C>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:118975199 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:118977225 C>T did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr7:48146662 C>G maps to NM_003364.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:158974403 G>C maps to NM_001135098.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:158980361 G>T maps to NM_001135098.1 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:74516240 C>T did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr16:21968569 C>G maps to NM_003366.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr1:229772213 T>C maps to NM_014777.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:229770870 G>T maps to NM_014777.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:229770686 G>A maps to NM_014777.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:229783476 C>G maps to NM_014777.2 S1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:229795040 C>G maps to NM_014777.2 A1524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr7:43916607 T>C maps to NM_001077663.1 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr9:131151542 G>A maps to NM_001135947.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:126202226 C>T maps to NM_001165974.1 W685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:126218238 C>T maps to NM_001165974.1 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr3:126218993 C>G maps to NM_001165974.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr3:126224832 A>G maps to NM_001165974.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:17554866 C>A maps to NM_153676.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr17:72915907 C>A maps to NM_173477.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:215955427 G>A maps to ENST00000366943 Q3566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr1:216424243 C>G did not map to a codon.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr1:216246231 T>G maps to ENST00000366943 A1952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:216017725 A>C maps to ENST00000366943 Y3056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr1:216062175 T>C maps to ENST00000366943 S2605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:215848718 A>T maps to ENST00000366943 P4178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr1:215848417 G>A maps to ENST00000366943 Q4279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:216465514 A>T did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr1:215821940 G>A maps to ENST00000366943 I4837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:216051222 C>T did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr1:216500969 G>A maps to ENST00000366943 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr1:216462639 A>T maps to ENST00000366943 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:216363667 T>A maps to ENST00000366943 V1431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:216073559 C>T did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr1:216143993 C>T maps to ENST00000366943 T2310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:215813993 G>A maps to ENST00000366943 N4958N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr1:215972467 C>A did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr1:215848478 T>C maps to ENST00000366943 T4258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:215916525 A>G maps to ENST00000366943 C3847C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:216500960 G>T maps to ENST00000366943 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr1:216166398 G>T maps to ENST00000366943 S2256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:216500990 C>A maps to ENST00000366943 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:17373366 C>T maps to NM_031941.3 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:47101574 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:47100994 A>T did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr23:47104081 A>G did not map to a codon.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr23:47101680 G>T did not map to a codon.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr23:47102050 C>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:47101704 G>T did not map to a codon.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr23:47104413 G>C did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr3:179426629 G>T maps to NM_003940.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:179460013 C>T maps to NM_003940.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr3:179501870 C>G maps to NM_003940.2 S845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr3:179481914 G>T maps to NM_003940.2 G740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr3:179447976 G>T maps to NM_003940.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:210395 C>A maps to NM_005151.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr12:62786901 A>T maps to ENST00000280377 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:62790073 G>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr21:30403060 T>C maps to NM_006447.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr21:30402982 G>T maps to NM_006447.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr21:30418999 C>T maps to NM_006447.2 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr8:11995030 G>C maps to NM_201402.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr22:18653533 C>T maps to NM_017414.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr22:18650676 G>T maps to NM_017414.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr1:161133755 C>T maps to NM_012475.4 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:20922415 G>A maps to ENST00000455117 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr1:55603511 C>A maps to NM_015306.2 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:55608722 C>A maps to NM_015306.2 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr1:55620439 T>A maps to NM_015306.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr1:55545264 A>G maps to NM_015306.2 H2382H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr21:17214735 A>C maps to ENST00000285681 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr21:17214841 G>T maps to ENST00000285681 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr21:17197356 G>A maps to ENST00000285681 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:132159855 C>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:132161298 G>T did not map to a codon.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr23:132160304 G>C did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:132161177 C>T did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:132162096 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:113704152 C>A maps to NM_020886.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr11:113679923 C>A maps to NM_020886.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57642682 C>T maps to NM_020903.2 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:57642467 G>T maps to NM_020903.2 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr19:57640073 C>T maps to NM_020903.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:57640424 G>T maps to NM_020903.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:109520494 G>T maps to NM_032663.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr12:109520715 G>A maps to NM_032663.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr12:109523483 C>T maps to NM_032663.3 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr16:23079560 C>A maps to NM_020718.3 G1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr17:58256731 G>A maps to NM_032582.3 Q1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr17:58260691 G>C maps to NM_032582.3 L1319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr1:78177449 T>C maps to NM_015017.3 E827E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr2:61459592 C>T maps to NM_014709.3 V2369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr2:61475682 T>A maps to NM_014709.3 T2119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr2:61463467 T>C maps to NM_014709.3 T2278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr2:61417462 T>A maps to NM_014709.3 L3272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:61439040 C>A maps to NM_014709.3 L2902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:76831521 G>A maps to NM_025090.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr17:76795028 G>A maps to NM_025090.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr17:76795010 G>A maps to NM_025090.3 D1073D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:219346934 G>A maps to NM_020935.2 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr2:219360481 C>T did not map to a codon.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:144109066 T>C maps to NM_032557.5 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:6183808 C>T maps to ENST00000404835 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr7:6189569 G>A maps to ENST00000404835 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr11:11977670 A>G maps to ENST00000399455 A1346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:22063026 T>C maps to NM_032236.5 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr1:22021657 T>C maps to NM_032236.5 Q928Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr1:22079069 C>T maps to NM_032236.5 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:41774220 C>T maps to ENST00000373009 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr12:6965208 G>A maps to NM_001098536.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:55513248 T>C did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:55513250 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:55514730 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:55514392 G>A did not map to a codon.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr10:75279615 G>A maps to NM_152586.3 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr10:75276615 G>A maps to NM_152586.3 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr17:5035696 G>A maps to NM_004505.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr10:11504811 A>T maps to NM_001080491.2 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr10:11505689 C>A maps to NM_001080491.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr16:8992279 G>A maps to NM_003470.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:50769123 C>T maps to NM_005154.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr15:50733608 G>A maps to NM_005154.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:41056654 G>C did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:41064717 G>C did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:41078485 T>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:41010251 G>C did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:40994070 G>T did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:41000370 C>A did not map to a codon.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr23:41075774 A>T did not map to a codon.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr23:41026798 C>T did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr24:14888736 A>G did not map to a codon.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr24:14922618 G>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr24:14959214 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:31233096 C>T maps to NM_005800.4 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:129053248 C>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:129058808 C>T did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:129059947 G>T did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:129063395 C>T did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:129055539 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:129059030 C>A did not map to a codon.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr23:129042040 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr13:52603077 G>T maps to NM_021645.5 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:72873703 A>G maps to NM_032175.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:72872775 G>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr5:72864309 A>G maps to NM_032175.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr5:72866450 G>A maps to NM_032175.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr17:49337957 C>A maps to NM_016001.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr12:101750710 C>T maps to NM_014503.2 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:101763602 G>A maps to NM_014503.2 L2163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr12:101721005 T>A maps to NM_014503.2 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr17:30214304 C>A maps to NM_018428.2 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr17:30213081 T>G did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr6:144768767 C>T maps to NM_007124.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:144860476 G>T maps to NM_007124.2 L2139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr6:145161968 G>T did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr6:144780309 C>A maps to NM_007124.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr6:144768370 G>T maps to NM_007124.2 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:144835119 C>T maps to NM_007124.2 L1674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:144820426 C>A maps to NM_007124.2 S1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr24:15372157 C>A did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr24:15448074 A>G did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr16:70818068 G>A maps to NM_018052.3 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:85820096 G>A maps to NM_006634.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:155149475 G>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr23:155127867 A>G did not map to a codon.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr23:155149500 G>T did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr23:155127862 C>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:116226634 C>T maps to NM_001172412.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr1:160394054 G>C maps to NM_020335.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr1:160389285 G>A maps to NM_020335.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:9954178 G>T maps to NM_003574.5 G286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr20:57009744 C>G maps to NM_004738.4 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:31753354 C>T maps to NM_006295.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr6:31749687 C>A maps to NM_006295.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr6:30892294 C>A maps to NM_001167734.1 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:213147328 C>A maps to NM_001136474.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr16:4431777 C>T maps to NM_138440.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr19:46021194 C>T maps to NM_003370.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr9:136661647 T>A did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr9:136671273 C>T maps to NM_001134398.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr9:136726512 C>A maps to NM_001134398.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr10:118895982 C>T maps to NM_001112704.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr23:154448553 T>C did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:154448555 G>A did not map to a codon.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr1:101188861 A>T maps to NM_001078.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr5:82815810 T>C maps to NM_004385.4 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr5:82849312 G>A maps to NM_004385.4 L3208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr5:82789634 G>T maps to NM_004385.4 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr5:82816284 C>A maps to NM_004385.4 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr9:35061052 C>A maps to NM_007126.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr9:35066807 C>T maps to NM_007126.3 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr8:67577945 A>G maps to NM_025054.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr8:67547089 C>T maps to NM_025054.4 Q1105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:6451847 C>A did not map to a codon.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr23:8433593 G>T did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr12:48238762 C>T maps to NM_001017535.1 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr12:48251017 C>G maps to NM_001017535.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr12:48249570 C>T maps to NM_001017535.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr4:177650745 G>C maps to NM_005429.2 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr4:177650828 G>C maps to NM_005429.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr10:135051451 C>T maps to NM_014468.2 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr10:135053755 G>T maps to NM_014468.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr3:157188204 C>A maps to NM_001167912.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:157081366 T>A maps to NM_001167912.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr3:157034970 T>G maps to NM_001167912.1 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr3:157099054 G>T maps to NM_001167912.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr17:56051848 T>C maps to NM_007146.2 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr23:135632947 G>A did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr23:135631088 G>A did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr3:10191555 G>A maps to NM_000551.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:219292726 G>A maps to NM_007127.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:219297586 T>C maps to NM_007127.2 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr10:17275866 T>A maps to NM_003380.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:153076433 C>A maps to NM_003381.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr14:77919735 C>T maps to ENST00000445370 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:77909005 C>A did not map to a codon.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:36986127 G>A maps to NM_053276.3 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr2:37041329 G>C maps to NM_053276.3 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:37002154 G>A maps to NM_053276.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr2:37032768 G>T maps to NM_053276.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr23:150573517 C>A did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:150572200 A>C did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr17:4689560 C>G maps to NM_182566.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57967656 G>A maps to NM_020633.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:53762719 T>C maps to NM_173856.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:53770582 C>T maps to NM_173857.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:53770078 G>T maps to NM_173857.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr1:247419830 T>A maps to NM_173858.1 L153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:247419471 T>A maps to NM_173858.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:247419657 C>G maps to NM_173858.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr1:247420095 T>A maps to NM_173858.1 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr6:133013652 G>C maps to NM_004666.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr6:133065440 A>G maps to NM_004665.2 *521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr6:133065516 G>T maps to NM_004665.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr6:133072502 G>T maps to NM_004665.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr6:133078686 T>A did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr6:133065474 T>C maps to NM_004665.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:51452137 A>G maps to ENST00000273612 N1259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr3:51475637 T>C maps to ENST00000273612 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr3:51475084 T>C maps to ENST00000273612 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr22:22599439 G>A maps to NM_007128.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr11:118939985 C>T maps to NM_021729.4 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr9:79996915 G>A maps to ENST00000376646 E3035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr8:100712131 T>C maps to NM_017890.3 L2167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:100568798 A>T maps to NM_017890.3 K1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr8:100779174 T>C maps to NM_017890.3 S2433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:100729550 G>T maps to NM_017890.3 E2228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr8:100732643 G>A maps to NM_017890.3 E2268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:100133570 G>T maps to NM_017890.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr8:100866425 G>A maps to NM_017890.3 A3628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr15:62223363 G>C maps to NM_020821.2 S1988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr15:62201243 T>G maps to NM_020821.2 A2975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr15:62228844 A>T maps to NM_020821.2 T1902T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr15:62219376 G>T maps to NM_020821.2 L2143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr15:62241689 C>A maps to NM_020821.2 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:12304674 G>A did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr1:12520421 G>A maps to NM_015378.2 V4211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:12567002 C>T maps to NM_015378.2 A4297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr1:12401885 G>C maps to NM_015378.2 L2892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:12318099 A>G maps to NM_015378.2 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr1:12402954 G>A did not map to a codon.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr1:12409359 G>A maps to NM_015378.2 V3120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr20:2840409 C>A maps to NM_022575.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr15:41192572 C>G maps to NM_020857.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr12:122745858 G>A maps to NM_022916.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr15:91550785 C>T maps to NM_018668.3 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:46697017 G>A maps to NM_018206.4 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr8:17137761 T>C maps to NM_152415.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr1:150048323 G>C maps to NM_007259.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr6:33232565 G>A maps to NM_022553.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr17:526853 A>C maps to NM_001128159.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr2:64169643 G>A maps to NM_016516.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:64148354 G>A maps to NM_016516.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:64160936 G>A maps to NM_016516.2 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr1:151156931 T>C maps to ENST00000354473 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr3:184675209 C>A maps to ENST00000437079 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr3:184580695 A>T maps to ENST00000437079 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr3:184586824 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:184648316 G>A maps to ENST00000437079 E953E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:184714181 G>C maps to ENST00000437079 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:58386587 T>C maps to NM_001130480.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr2:58366798 A>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:107316489 C>A did not map to a codon.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr11:124617489 T>A maps to NM_014312.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:65252572 G>T did not map to a codon.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr23:65247898 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:65252492 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:65242193 C>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:65252401 G>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:159827691 C>T maps to NM_001013661.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr2:17773401 G>T maps to NM_003385.4 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr19:54567013 G>C maps to NM_198481.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:54617573 C>T maps to ENST00000404951 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr7:54617717 G>T maps to ENST00000404951 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr14:74711939 T>C maps to NM_182894.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr1:1372496 C>T maps to NM_022834.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:116038535 C>T maps to NM_198496.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:98852941 T>G did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:98744740 G>T maps to NM_144992.4 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr2:98736130 C>T maps to NM_144992.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr2:98844702 G>A maps to NM_144992.4 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr11:123995011 A>G maps to NM_014622.4 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:123989017 G>A maps to NM_014622.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:49842318 G>T maps to NM_198570.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:215279216 G>A maps to NM_001080500.2 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:215440411 A>T maps to NM_001080500.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr11:61050267 G>A maps to NM_152718.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:6125938 G>A maps to NM_000552.3 F1717F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr12:6085426 C>T did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr12:6184681 G>A maps to NM_000552.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr12:6125731 A>T maps to NM_000552.3 L1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr12:6132839 G>T maps to NM_000552.3 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr12:6138584 G>A maps to NM_000552.3 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr12:6061008 C>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:28905254 C>T maps to NM_016628.3 H570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr10:28900817 G>A maps to NM_016628.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr14:100803431 G>T maps to NM_173701.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:100828123 T>C maps to NM_173701.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr1:119584927 G>A maps to NM_015836.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:48542348 T>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:48549499 G>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:48542367 A>G did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:48545325 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:110424669 C>T maps to NM_003931.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr12:14949740 C>T maps to NM_016312.2 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr12:14947513 G>A maps to NM_016312.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr22:42423061 G>A maps to NM_152613.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:42423025 C>T maps to NM_152613.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr13:41642709 A>G maps to NM_007187.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr7:70853219 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr7:71135072 T>C maps to NM_022479.1 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr7:71175876 C>A maps to NM_022479.1 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr7:71175783 T>G maps to NM_022479.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr7:70885947 C>G maps to NM_022479.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr7:70880935 G>A maps to NM_022479.1 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:71177091 C>A maps to NM_022479.1 C586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:70885908 A>T maps to NM_022479.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr7:73105282 A>T maps to ENST00000423497 K134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr7:73279345 C>A maps to NM_182504.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr2:224809974 C>T maps to NM_020830.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr4:85750242 G>A maps to NM_014991.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr4:85598452 C>G maps to NM_014991.4 V3452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr4:85687026 G>A maps to NM_014991.4 L1708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr4:85664937 C>T maps to NM_014991.4 R1996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5036-01A-01D-1441-08 chr4:85771052 A>G did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr4:85750300 G>C maps to NM_014991.4 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:55458023 G>T maps to NM_007086.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr4:10080564 C>A maps to NM_017491.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr10:122664829 G>A did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr10:122666348 G>T maps to NM_018117.11 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr23:48463412 A>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:9538774 G>A maps to NM_145054.4 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr17:9490040 G>A maps to NM_145054.4 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:177061073 G>A maps to NM_170710.4 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:177073060 C>T maps to NM_170710.4 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr4:177071096 T>A maps to NM_170710.4 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2755-01A-01D-1522-08 chr4:177098241 T>A maps to NM_170710.4 P1200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr19:994261 G>A maps to NM_024100.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr4:39241944 T>C maps to NM_025132.3 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr14:102606454 C>A maps to ENST00000454394 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr14:102675625 C>A maps to ENST00000454394 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:735760 G>A maps to ENST00000248142 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr1:224577559 C>A maps to NM_025160.6 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr9:116082636 C>G maps to NM_001012361.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr2:128471305 C>A maps to NM_018383.4 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr2:128471190 C>A maps to NM_018383.4 E1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr2:20137517 G>T maps to NM_001006657.1 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr2:20137622 G>A maps to NM_001006657.1 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr2:20131146 T>C maps to NM_001006657.1 K960K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr5:110443092 C>G maps to NM_139281.2 Y483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr21:44273747 C>T maps to NM_018669.4 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr5:76728961 A>G maps to NM_018268.2 *460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:29145783 G>A did not map to a codon.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr2:29152476 T>C maps to NM_015131.1 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:117540901 A>G did not map to a codon.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:117576643 G>T did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:117527018 C>G did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr23:117540952 G>T did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:117566798 G>C did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr23:48932916 C>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:48935747 G>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:48933066 G>T did not map to a codon.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr17:80575230 G>A maps to NM_019613.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr17:80575269 G>A maps to NM_019613.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr6:33254659 A>G maps to NM_005452.5 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:167245806 T>C did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr3:167293741 T>A maps to NM_178824.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:167248975 C>T maps to NM_178824.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr3:113146060 G>A maps to NM_001164496.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr3:113135374 G>T maps to NM_001164496.1 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:113138898 G>A maps to NM_001164496.1 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr2:74652763 C>A maps to NM_032118.2 S314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr5:140048088 T>C did not map to a codon.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr7:158723179 T>C maps to NM_018051.4 H840H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr7:158719681 G>A did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr7:158718959 C>T maps to NM_018051.4 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr7:158705761 G>T maps to NM_018051.4 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr19:36557156 A>G did not map to a codon.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr19:36549713 C>A maps to NM_001083961.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr19:36546011 C>T maps to NM_001083961.1 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr1:85559203 C>A maps to NM_145172.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr1:241929536 A>G maps to NM_144625.4 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:241901792 T>C did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:43649506 C>A maps to NM_001195831.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr8:124157049 G>T maps to NM_145647.3 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr8:124146370 A>T maps to NM_145647.3 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:54424310 C>T maps to NM_015285.2 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr18:54398665 T>C maps to NM_015285.2 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr15:54007543 C>A maps to NM_182758.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr15:53908392 C>T maps to NM_182758.2 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr15:53907986 C>A maps to NM_182758.2 G806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr15:53907737 C>A maps to NM_182758.2 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr15:53889378 G>T maps to NM_182758.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr15:54007483 A>G maps to NM_182758.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:190331240 C>G maps to NM_032168.1 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:44143305 G>T maps to NM_024908.3 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:67292638 C>A maps to NM_024763.4 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:67337154 T>A maps to NM_024763.4 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr1:3553569 G>A maps to NM_017818.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:151093116 C>T maps to ENST00000426624 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr19:33628617 T>A maps to NM_173479.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr16:711940 G>C maps to NM_145294.4 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr7:134881004 G>T maps to NM_014149.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr15:90258208 A>T did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr1:27618777 G>T maps to ENST00000319394 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr1:27608756 G>T maps to ENST00000319394 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:141420745 T>A maps to NM_001105558.1 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:141429328 A>C did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr7:141408803 G>A maps to NM_001105558.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr20:44180701 G>C maps to NM_130896.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:48917206 C>T maps to NM_175575.5 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr17:48917536 G>A maps to NM_175575.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr4:1920070 A>T maps to NM_133335.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr8:38189053 C>A maps to NM_023034.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr8:38162107 T>A maps to NM_023034.1 R870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr8:38133957 G>A maps to NM_023034.1 R1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr4:1993338 G>T maps to NM_005663.3 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr12:65461473 C>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:175437022 C>A maps to NM_003387.4 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:38421163 C>T maps to NM_133264.4 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr7:29928943 G>A maps to NM_001080529.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:5262286 C>A maps to NM_015610.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:15535690 G>T maps to ENST00000389282 R1445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr1:68697928 A>G maps to NM_024911.6 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr12:1017900 C>T maps to NM_001184985.1 I2624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr12:994799 G>T maps to NM_001184985.1 V1870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr12:1005491 C>T maps to NM_001184985.1 Q2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr12:994442 A>G maps to NM_001184985.1 S1751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr12:1005367 G>C maps to NM_001184985.1 V2165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:991097 A>C maps to NM_001184985.1 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr12:994584 G>T maps to NM_001184985.1 G1799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:54276064 G>T did not map to a codon.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr23:54275553 G>A did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:54337674 T>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:54334464 C>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:54359718 C>T did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr23:54321215 A>G did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:54264799 C>A did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:54265523 G>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:54321178 A>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:54275802 C>A did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr23:54275130 T>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr17:40936149 C>T maps to NM_032387.4 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr17:40937113 G>C did not map to a codon.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr7:120969746 C>G maps to NM_057168.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr7:116955160 G>T maps to NM_003391.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr7:116960738 G>A maps to NM_003391.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr7:116955271 G>A maps to NM_003391.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr1:228210541 C>T maps to ENST00000366753 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:1749039 G>A maps to NM_032642.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr3:13921277 G>C maps to NM_004625.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr22:46327058 G>T maps to NM_058238.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr5:137424655 G>T maps to NM_058244.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:228109219 C>G maps to NM_003395.2 *366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr17:44950020 C>T maps to NM_003396.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr8:31024622 A>G maps to NM_000553.4 K1356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr8:31015035 C>G maps to NM_000553.4 P1324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr12:108589758 G>A maps to ENST00000261400 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr11:32450094 G>A maps to NM_024426.4 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr11:32439175 G>T maps to NM_024426.4 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr11:32417923 C>A maps to NM_024426.4 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr6:160176216 A>T maps to NM_004906.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr5:167850746 C>G maps to NM_001161661.1 S495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr4:184233498 A>G maps to ENST00000448232 E1154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr4:184182540 G>T maps to ENST00000448232 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr23:10047793 G>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:10096088 A>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:10109497 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:79245629 C>G maps to NM_016373.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr8:87424103 G>T did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr16:69874129 C>T maps to NM_007014.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5592-01A-01D-1632-08 chr3:149290744 C>G maps to NM_001168278.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr3:149374961 C>A maps to NM_001168278.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2792-01A-01D-0983-08 chr19:7685167 C>T maps to NM_020196.2 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr23:52893868 C>G did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:52895511 G>A did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:52841654 C>T did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr23:52841663 T>C did not map to a codon.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr2:31598421 T>A did not map to a codon.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr2:31572969 C>A maps to NM_000379.3 G917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr2:31588975 C>G did not map to a codon.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:123019958 A>G did not map to a codon.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr23:123040951 A>G did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:123034477 C>T did not map to a codon.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr23:123019781 C>A did not map to a codon.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr23:123020330 G>A did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:123034380 A>G did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:39228797 G>T maps to NM_194293.2 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr3:39228400 G>A maps to NM_194293.2 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2715-01A-01D-1522-08 chr3:39227576 G>A maps to NM_194293.2 V1120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr3:39229919 A>G maps to NM_194293.2 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:168103269 C>T maps to NM_152381.5 L1790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:168108254 C>T maps to NM_152381.5 F3451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr2:168100235 G>T maps to NM_152381.5 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr2:168108096 G>T maps to NM_152381.5 E3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:168103508 A>T maps to NM_152381.5 L1869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:168104216 G>T maps to NM_152381.5 L2105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:168106413 G>T maps to NM_152381.5 E2838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr2:168102848 T>A maps to NM_152381.5 A1649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr2:168104240 C>A maps to NM_152381.5 S2113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr2:168099527 C>A maps to NM_152381.5 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr2:168107063 C>A maps to NM_152381.5 S3054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr2:167760265 C>A maps to NM_152381.5 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr2:168102210 C>T maps to NM_152381.5 R1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:167760267 G>T maps to NM_152381.5 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr2:168097246 G>A did not map to a codon.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr2:168108053 G>T maps to NM_152381.5 T3384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr2:168107681 G>A maps to NM_152381.5 E3260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr2:168105056 G>A maps to NM_152381.5 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2781-01A-01D-1522-08 chr2:168105152 T>A maps to NM_152381.5 G2417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr2:168100712 T>C maps to NM_152381.5 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr23:37587031 G>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:37553743 C>A did not map to a codon.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr23:37587106 A>T did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr23:37545360 G>T did not map to a codon.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr22:17288959 C>A maps to NM_175878.3 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:56436230 G>A maps to NM_052898.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr8:56436017 G>A maps to NM_052898.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr8:10756094 A>G maps to NM_173683.3 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:100170052 G>A did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:100169713 G>T did not map to a codon.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:14211998 G>T maps to NM_004628.4 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr10:111667493 G>A maps to NM_020383.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr23:128902322 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:128886217 A>G did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr23:128879189 C>A did not map to a codon.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr23:128885769 T>C did not map to a codon.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr23:128887224 G>A did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr22:41265119 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:21417151 A>C maps to NM_022459.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr13:21442735 C>T maps to NM_022459.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr13:21396421 G>A maps to NM_022459.4 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr13:21436983 C>A maps to NM_022459.4 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:43534989 G>T maps to NM_020750.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr16:28109924 C>A maps to NM_015171.2 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr16:28124344 C>T maps to NM_015171.2 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr1:180832868 G>T maps to NM_004736.3 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr5:82499433 G>C maps to NM_022406.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:82554406 A>T maps to NM_022406.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr22:42042980 A>C maps to NM_001469.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr22:42018067 A>G maps to NM_001469.3 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:42042908 G>A maps to NM_001469.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr12:58340810 A>G maps to NM_033276.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr3:142037718 T>C maps to NM_019001.3 L1476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:21349206 C>T maps to NM_012255.3 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr20:21314741 C>T maps to NM_012255.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:38401829 G>A maps to NM_005108.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr3:38415992 G>T maps to NM_005108.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr16:17202562 G>T maps to NM_022166.3 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:17211611 C>G maps to NM_022166.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr1:33244984 G>A maps to NM_003680.3 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr12:32906868 C>A maps to NM_001040436.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr12:32902908 A>G maps to NM_001040436.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:183524832 C>T maps to NM_018023.4 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:183433027 G>A maps to NM_018023.4 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr18:743304 G>A maps to NM_005433.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:38799947 G>A maps to NM_001039672.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr6:43480207 G>A maps to ENST00000506469 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr2:32517244 G>T did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr4:44631419 C>G maps to NM_182592.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:44626799 C>A did not map to a codon.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr4:44638038 C>A maps to NM_182592.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr14:75283755 C>T maps to NM_019589.2 D1936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr14:75302032 C>T maps to NM_019589.2 V2120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:75265977 G>T maps to NM_019589.2 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr14:75284932 G>A did not map to a codon.
Sequencing variant TCGA-46-3767-01A-01D-0983-08 chr14:75269257 G>A did not map to a codon.
Sequencing variant TCGA-56-5898-01A-11D-1632-08 chr14:75265314 A>G maps to NM_019589.2 A1105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr14:75276444 A>T maps to NM_019589.2 P1628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr10:27425294 A>C maps to NM_139312.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:207222724 G>T maps to NM_018566.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr22:22064997 C>T maps to NM_013313.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr17:57474473 G>T maps to NM_001005404.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:30379531 C>T maps to NM_001127399.1 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:135745406 C>T maps to NM_025052.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:135744572 T>C maps to NM_025052.3 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr2:135745181 A>T maps to NM_025052.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr2:135741287 T>C maps to NM_025052.3 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr2:135744461 A>T maps to NM_025052.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr2:135744863 A>G maps to NM_025052.3 N526N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr4:69188477 C>T maps to NM_001031732.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr5:112870076 G>A maps to NM_022828.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr20:61833926 G>A maps to NM_017798.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr1:29070236 G>T maps to NM_016258.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr17:1303365 C>A maps to NM_006761.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr17:1265200 A>G maps to NM_006761.4 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:155644851 G>A maps to ENST00000368339 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:21875390 G>A did not map to a codon.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr7:100346013 G>T maps to ENST00000349350 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:100358099 G>T maps to ENST00000349350 T1261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr7:100364684 C>A maps to ENST00000349350 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr7:100366311 C>A maps to ENST00000349350 A1707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr7:100349595 C>G maps to ENST00000349350 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr7:100349950 C>A maps to ENST00000349350 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr2:98351160 G>C maps to NM_001079.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr2:98341706 C>A maps to NM_001079.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr3:167016090 A>T did not map to a codon.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr3:167016198 A>T maps to ENST00000307529 Y591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:166960327 T>C maps to ENST00000307529 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:167000261 G>T maps to ENST00000307529 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:2408484 G>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:2408625 G>A did not map to a codon.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr22:50278005 T>G maps to NM_014838.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:50279760 G>A maps to NM_014838.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:56186894 G>A maps to NM_030776.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr14:64988812 C>T maps to NM_001123329.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr14:64989631 T>C maps to NM_001123329.1 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr8:81412555 A>G maps to NM_001105539.1 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr3:101383875 G>A maps to NM_014415.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:101384598 G>A maps to NM_014415.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr11:114121264 G>T maps to NM_001018011.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr3:114070441 G>A maps to NM_001164342.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr3:114070354 C>T maps to NM_001164342.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr3:114070036 C>T maps to NM_001164342.1 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:114069244 C>A maps to NM_001164342.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr6:109802863 T>A maps to NM_014797.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr6:109797402 T>C maps to NM_014797.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr6:109796670 C>A maps to NM_014797.2 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:109787324 G>C maps to NM_014797.2 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr11:62520527 G>A maps to NM_024784.3 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:119387960 C>A did not map to a codon.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr9:129642901 C>T maps to ENST00000319119 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr3:141164622 C>A maps to NM_001080412.2 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr3:141161799 A>G maps to NM_001080412.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr3:141164614 C>T maps to NM_001080412.2 Q1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr12:57398014 G>A maps to NM_014830.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr17:7365285 C>T maps to NM_020899.3 E1005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr20:62407097 G>A maps to NM_025224.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr1:6648819 G>T maps to NM_005341.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr1:6642199 C>G maps to NM_005341.2 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:154988917 C>T maps to ENST00000417934 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr1:37947223 G>T maps to NM_025079.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr23:64722204 C>A did not map to a codon.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr23:64723016 G>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:64709194 G>T did not map to a codon.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:64721935 T>C did not map to a codon.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr13:46549560 T>C maps to ENST00000242848 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr14:89037426 G>C did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr2:187368928 A>G maps to NM_018471.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr2:187368898 G>A maps to NM_018471.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr16:88691008 G>C did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr16:88697586 C>A maps to ENST00000452588 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr8:144621137 A>C maps to NM_015117.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr8:144550571 C>T maps to NM_015117.2 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:144620615 C>T maps to NM_015117.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:47570092 G>A maps to NM_015168.1 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:113089965 G>A maps to NM_198581.2 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr16:11859380 G>T maps to NM_014153.3 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr22:41716690 C>T maps to ENST00000351589 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr22:41751775 G>A maps to ENST00000351589 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr22:41745267 C>T maps to ENST00000351589 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr23:64138986 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:64137743 C>A did not map to a codon.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr23:64137692 G>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:64137713 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:64141825 C>A did not map to a codon.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr23:64138931 G>T did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:64137705 C>A did not map to a codon.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr23:64141802 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:52956402 C>A did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:117959987 T>A did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr23:117959764 G>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:117959683 T>A did not map to a codon.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr23:117960243 G>T did not map to a codon.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr23:73524597 A>T did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:73524495 G>A did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:111698771 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:111698733 C>G did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:111698021 T>A did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:111698849 T>G did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr18:60241356 C>G maps to NM_017742.4 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr18:60242386 G>T maps to NM_017742.4 G1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr18:60223501 C>T maps to NM_017742.4 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr10:81154190 G>C maps to NM_153367.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr20:279138 G>T maps to NM_033089.6 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:77913753 G>T did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr23:77912827 C>A did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:77912920 A>C did not map to a codon.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr5:80604813 G>A maps to NM_032280.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:99999548 C>T maps to NM_017984.3 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr3:28454870 A>T maps to NM_001040432.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr2:207146626 G>T maps to NM_020923.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr2:207172251 A>C maps to NM_020923.1 T1000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr2:207176076 A>T maps to NM_020923.1 P2275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr2:207170434 C>T maps to NM_020923.1 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr2:207169470 T>A maps to NM_020923.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr2:207176005 A>T maps to NM_020923.1 K2252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr5:822004 C>A maps to NM_024786.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr5:850699 C>A maps to NM_024786.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr6:158014098 G>T maps to NM_024630.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:74644525 A>C did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:74641768 C>A did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:74649008 G>T did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:74644567 C>A did not map to a codon.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr3:195937538 G>T maps to NM_001039617.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr3:195937562 G>A maps to NM_001039617.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr8:17053098 G>A maps to NM_016353.4 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr13:21976985 T>C maps to ENST00000400590 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr9:14619680 C>G did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:6624665 G>T maps to NM_018106.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr11:57464263 G>A maps to NM_015457.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr22:20126806 C>T maps to NM_013373.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr22:20132767 A>T maps to NM_013373.3 K715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr22:20128225 G>T maps to NM_013373.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5784-01A-01D-1632-08 chr23:128940417 G>T did not map to a codon.
Sequencing variant TCGA-22-5482-01A-01D-1632-08 chr23:128957693 G>A did not map to a codon.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr23:128946744 C>A did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:128957774 G>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr10:31810368 A>G maps to NM_001174096.1 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr10:31803580 T>C maps to NM_001174096.1 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr10:31809072 C>T maps to NM_001174096.1 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr2:145157427 C>T maps to NM_014795.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr2:145156419 G>A maps to NM_014795.3 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr2:145161577 C>A maps to NM_014795.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr7:1197327 T>C maps to ENST00000401903 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr2:220072368 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:74970880 A>T maps to ENST00000437241 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1071-01A-01D-1521-08 chr8:135614755 C>T maps to NM_020863.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:135614254 G>A maps to NM_020863.3 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:135524748 C>A maps to NM_020863.3 A1110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr8:135524757 C>A maps to NM_020863.3 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr8:135669837 T>A maps to NM_020863.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2800-01A-01D-1267-08 chr8:135613996 C>A maps to NM_020863.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr12:72057375 A>G maps to NM_144982.4 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr16:72992280 C>T maps to NM_006885.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr16:72984562 C>T maps to NM_006885.3 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2709-01A-21D-1817-08 chr16:72828129 G>A maps to NM_006885.3 S2817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr16:72992121 C>T maps to NM_006885.3 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr8:77767133 G>A maps to NM_024721.4 R2659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr8:77618477 C>T maps to NM_024721.4 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr8:77775399 C>A maps to NM_024721.4 L3150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr8:77768504 C>A maps to NM_024721.4 S3116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:77616802 C>A maps to NM_024721.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:77768486 C>A maps to NM_024721.4 P3110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:77763548 C>T maps to NM_024721.4 P1464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:77765672 T>G maps to NM_024721.4 V2172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr8:77767034 G>A maps to NM_024721.4 L2626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr8:77761752 T>A maps to NM_024721.4 Y1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr8:77767220 G>T maps to NM_024721.4 S2688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr8:77775916 C>T maps to NM_024721.4 Q3323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr8:77618551 C>A maps to NM_024721.4 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr8:77616389 G>T maps to NM_024721.4 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr8:77616922 C>G maps to NM_024721.4 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr8:77767224 T>C maps to NM_024721.4 L2690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:77767032 C>T maps to NM_024721.4 L2626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr8:77620258 C>T maps to NM_024721.4 H1023H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:77767922 A>G maps to NM_024721.4 K2922K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr8:77617651 C>T maps to NM_024721.4 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr8:77766791 G>A maps to NM_024721.4 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr8:77765709 C>A maps to NM_024721.4 R2185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr8:77763195 G>T maps to NM_024721.4 E1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr8:77765849 G>A maps to NM_024721.4 T2231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr8:77764394 G>A maps to NM_024721.4 T1746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr15:42710094 G>A maps to NM_022473.1 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr15:42742494 T>A maps to NM_022473.1 R636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:42710038 G>A maps to NM_022473.1 C1853C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:42727710 C>T maps to NM_022473.1 R1561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr15:42742723 G>T maps to NM_022473.1 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr15:42742429 T>C maps to NM_022473.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:44832206 G>T maps to ENST00000412927 Y718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:44833688 G>T maps to ENST00000412927 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6771-01A-11D-1817-08 chr19:36853128 T>A maps to NM_020917.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:57065665 C>T maps to NM_020828.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:38127105 A>G maps to NM_014898.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:39898387 C>A maps to NM_003407.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr2:43452888 T>A maps to NM_006887.4 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr9:115805910 G>T maps to NM_003408.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:144332174 T>G maps to NM_173832.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr4:188924185 C>A maps to NM_174900.3 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr6:29640951 C>T maps to NM_001109809.2 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr6:29640397 C>T maps to NM_001109809.2 W497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:36884092 G>A maps to NM_133466.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr16:68591959 C>T maps to NM_133458.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr16:68598586 C>A maps to NM_133458.2 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr16:68597568 T>C maps to NM_133458.2 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr16:68598058 G>T maps to NM_133458.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr11:58384715 G>A maps to NM_053023.4 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr11:58385038 C>A maps to NM_053023.4 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr11:64854842 A>C maps to NM_006782.3 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr8:106810991 G>T maps to NM_012082.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr8:106815540 G>T maps to NM_012082.3 S1077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr8:106814721 G>T maps to NM_012082.3 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr8:106801084 G>T maps to NM_012082.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr8:106813737 C>T maps to NM_012082.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr8:106815441 G>A maps to NM_012082.3 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:106431475 G>T maps to NM_012082.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr5:32395263 C>T did not map to a codon.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr23:24197617 C>A did not map to a codon.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr24:2829518 A>T did not map to a codon.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr24:2843673 C>T did not map to a codon.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr14:73459961 A>G maps to NM_021260.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr14:73442324 C>T maps to NM_021260.2 K580K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr14:73442366 G>A maps to NM_021260.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr14:68256123 G>A maps to NM_015346.3 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr14:68265177 C>A maps to NM_015346.3 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr14:68248187 C>T maps to NM_015346.3 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr14:68249613 C>A maps to NM_015346.3 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr14:68274247 C>G maps to NM_015346.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr14:68249977 G>C maps to NM_015346.3 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr14:68220847 G>T maps to NM_015346.3 T2356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr14:68275997 G>T maps to NM_015346.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr14:68234441 C>A maps to NM_015346.3 R1923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr4:2306647 G>A maps to NM_020972.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr4:2306728 C>A maps to NM_020972.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr4:2343207 G>A maps to NM_020972.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr4:2307004 G>A maps to NM_020972.2 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr4:2274975 C>G maps to NM_020972.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:52769497 C>T maps to NM_004799.2 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr1:52703868 G>A maps to NM_004799.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr20:62340456 G>A maps to NM_032527.4 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr8:123964388 A>G maps to NM_014943.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr8:123964739 G>A maps to NM_014943.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr8:123964706 C>T maps to NM_014943.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:123964727 G>A maps to NM_014943.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr8:123964394 C>T maps to NM_014943.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr3:147128168 C>T maps to NM_003412.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr3:147128211 C>A maps to NM_003412.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr3:147128642 C>A maps to NM_003412.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr3:147128270 G>A maps to NM_003412.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr3:147130323 C>A maps to NM_003412.3 C334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:147128489 C>G maps to NM_003412.3 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr3:147128090 C>T maps to NM_003412.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr13:100637596 G>A maps to NM_007129.2 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr13:100637326 C>A maps to NM_007129.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:136648862 C>A did not map to a codon.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr23:136649617 C>A did not map to a codon.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr23:136649887 G>C did not map to a codon.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr23:136648936 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr23:136649362 G>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:136649892 A>G did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr3:147109007 G>A maps to NM_001168379.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr3:147114107 C>T maps to NM_001168379.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr3:147113819 G>T maps to NM_001168379.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:147113642 G>A maps to NM_001168379.1 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:58100029 C>T maps to NM_001010879.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:58099929 C>A maps to NM_001010879.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:58101881 G>T maps to NM_001010879.2 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:58101643 G>A maps to NM_001010879.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr19:57286631 G>A maps to NM_001146326.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:57646927 G>T maps to NM_052882.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:57646493 G>C maps to NM_052882.1 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:99631579 G>T maps to NM_003439.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr6:28327629 G>T maps to NM_024493.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr6:28327434 C>T maps to NM_024493.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr6:28213022 A>G maps to NM_019110.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr6:28213600 G>A maps to NM_019110.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:99129344 G>T maps to NM_014569.3 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:101153009 A>G did not map to a codon.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr23:101139357 G>T did not map to a codon.
Sequencing variant TCGA-39-5028-01A-01D-1441-08 chr23:101139089 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:101138537 C>G did not map to a codon.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr23:101159198 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:140080050 G>T maps to NM_144723.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr3:178785486 C>A maps to NM_022470.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr13:20567802 G>A maps to NM_001190965.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr23:70464693 C>A did not map to a codon.
Sequencing variant TCGA-22-5480-01A-01D-1632-08 chr23:70466472 G>C did not map to a codon.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:70469502 G>A did not map to a codon.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr23:70468980 G>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:70472624 C>T did not map to a codon.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr23:70466281 C>G did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:70472961 A>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:70469494 T>G did not map to a codon.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr23:70472741 C>T did not map to a codon.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr13:20413086 G>A maps to NM_001142684.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr1:35469606 C>A did not map to a codon.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr1:42898959 C>A did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr17:4644068 G>T maps to NM_001136046.1 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr20:45865219 G>T maps to ENST00000471951 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr20:45905322 G>A maps to ENST00000471951 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr20:45976615 G>A maps to ENST00000471951 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr12:133733274 G>A maps to NM_015394.4 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr19:21910558 G>T maps to NM_173531.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr19:21910570 T>A maps to NM_173531.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr7:64167218 G>A maps to NM_016220.3 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2725-01A-01D-1267-08 chr7:64167833 T>G maps to NM_016220.3 Y384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr7:64168412 G>A maps to NM_016220.3 E577E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:48789339 T>A maps to NM_153608.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr7:64439245 T>A maps to NM_015852.3 K235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr5:43175066 C>A maps to ENST00000509156 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr20:18296592 G>A maps to ENST00000401790 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:58579502 G>T maps to NM_007134.1 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr19:58579627 G>T maps to NM_007134.1 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr19:58573066 C>A maps to NM_007134.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr19:58579129 C>T maps to NM_007134.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr19:12298582 C>A maps to NM_003437.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr4:367491 C>T maps to NM_003441.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr4:366585 G>A maps to NM_003441.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr19:36727714 G>T maps to NM_007145.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:124952366 C>A maps to NM_021964.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr3:124998069 C>A maps to NM_021964.2 G161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr19:44500910 C>G maps to NM_003445.2 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:47271925 C>A did not map to a codon.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr8:146156984 C>T maps to NM_006958.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr19:53572221 G>C maps to NM_001102603.1 S522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr6:28053317 G>A maps to NM_003447.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr6:28056491 G>A maps to NM_003447.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr6:28053948 G>A did not map to a codon.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr9:97054699 C>G maps to NM_194320.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:97063486 C>T maps to NM_194320.2 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr9:97062613 G>T maps to NM_194320.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr16:3452088 G>T maps to NM_003450.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:52090505 G>T maps to NM_007147.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:35231909 A>G maps to ENST00000392232 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr23:47836918 T>C did not map to a codon.
Sequencing variant TCGA-66-2778-01A-02D-1522-08 chr6:27420014 A>T maps to NM_007149.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:152128348 A>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:152087622 G>T did not map to a codon.
Sequencing variant TCGA-66-2793-01A-01D-1267-08 chr23:152087615 A>G did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr9:104171501 T>C maps to NM_003452.2 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr6:28195518 C>T maps to ENST00000425468 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr6:28200374 C>T maps to ENST00000425468 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr11:3392295 G>A maps to NM_001130520.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr3:44670822 C>T maps to NM_006991.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr19:12243725 A>G maps to NM_021143.2 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:12243920 T>C maps to NM_021143.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr19:12244328 C>T maps to NM_021143.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr16:3274469 G>A maps to NM_198088.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr11:123597133 T>C maps to NM_003455.2 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr11:123599837 G>C maps to NM_003455.2 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr16:3169512 G>A maps to NM_001042428.1 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:22154212 C>T maps to NM_007153.3 W1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr19:22156605 T>G maps to NM_007153.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:22156017 C>T maps to NM_007153.3 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:22154163 G>T maps to NM_007153.3 P1224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr19:22154700 A>C maps to NM_007153.3 T1045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:22156134 G>T maps to NM_007153.3 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:22155699 C>T maps to NM_007153.3 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr16:3187643 G>A maps to NM_001134655.1 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr19:44536823 C>T maps to NM_001129996.1 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:44571243 C>G maps to NM_013361.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:44622461 C>A maps to NM_013362.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:44738911 C>G maps to NM_182490.1 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr19:44932747 G>A maps to NM_014518.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:44934256 G>A maps to NM_014518.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr16:71482505 T>C maps to NM_145911.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr16:71482586 G>A maps to NM_145911.1 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr16:71483755 C>A maps to NM_145911.1 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr16:71483408 T>C maps to NM_145911.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr17:5009780 C>A maps to NM_014519.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:44777880 T>A maps to NM_181756.1 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr19:44660427 G>T maps to NM_006630.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr18:74649196 G>T maps to NM_007345.3 S1558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr18:74580736 C>T maps to NM_007345.3 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1078-01A-01D-1521-08 chr18:74620296 C>G maps to NM_007345.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr18:74563728 A>G did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr18:74631814 G>T maps to NM_007345.3 E1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr18:74639005 G>C maps to NM_007345.3 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr18:74622033 G>T maps to NM_007345.3 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr1:244218489 G>T maps to NM_205768.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr1:244218144 G>T maps to NM_205768.2 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr8:146106967 C>A maps to NM_021061.3 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr8:146108174 C>T maps to NM_021061.3 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr8:145947100 T>C maps to NM_138367.1 K648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:20002736 C>G maps to NM_021047.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr19:24309054 G>C did not map to a codon.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:24309707 A>G maps to NM_203282.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:22255655 G>T maps to NM_033468.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5478-01A-01D-1632-08 chr19:22271748 C>T maps to NM_033468.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr19:57723616 A>T maps to NM_003417.4 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:57723830 G>T maps to NM_003417.4 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr16:31925795 G>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:31927419 C>G maps to NM_003414.4 S617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:58723024 G>T maps to NM_133502.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:152612880 C>T did not map to a codon.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr23:152613050 G>A did not map to a codon.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr23:152612646 G>A did not map to a codon.
Sequencing variant TCGA-22-0944-01A-01D-1521-08 chr16:89789137 C>G maps to NM_001113525.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr16:89799887 A>T did not map to a codon.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr7:111936010 T>C maps to NM_021994.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:53304794 C>T maps to NM_006969.3 W101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:53303165 G>A maps to NM_006969.3 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr19:53303426 C>T maps to NM_006969.3 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr22:22869795 T>C maps to NM_080740.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr22:22869713 G>A maps to NM_080740.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5492-01A-01D-1632-08 chr23:129394397 G>T did not map to a codon.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr23:129394413 C>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr15:56968993 T>C maps to NM_017661.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2707-01A-01D-1522-08 chr15:56981652 G>T maps to NM_017661.2 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr15:56981256 A>G maps to NM_017661.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr1:200377462 T>C maps to NM_012482.3 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr1:200378068 G>T maps to NM_012482.3 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:44891929 G>T maps to NM_152354.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr17:15619752 G>T maps to NM_020652.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr17:15619582 C>G maps to NM_020652.2 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr6:87971381 G>T maps to NM_015021.1 E2679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr6:87967474 C>A maps to NM_015021.1 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr6:87969103 A>G maps to NM_015021.1 L1919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr6:87969025 A>G maps to NM_015021.1 Q1893Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr21:43412302 G>T maps to NM_020727.4 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr7:99669783 G>T maps to NM_032924.3 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr19:35435154 G>T maps to NM_001099438.1 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr5:150275762 A>T maps to NM_001172831.1 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr6:28966577 C>G maps to NM_001010877.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:9271286 C>T maps to NM_020933.4 I322I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-37-4133-01A-01D-1352-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr6:43316085 C>T maps to NM_014345.2 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:53384205 G>C maps to NM_207333.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr6:28294227 T>A maps to NM_030899.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr6:28297318 G>A maps to NM_030899.4 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5022-01A-21D-1817-08 chr19:58982275 G>C maps to NM_014347.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:58966988 A>G maps to NM_207395.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:58639457 G>T maps to NM_024620.3 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr19:58639466 G>T maps to NM_024620.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr19:58639613 C>T maps to NM_024620.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:54080615 G>T maps to NM_001079907.1 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:14805851 G>T maps to NM_032433.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr20:45131353 C>A maps to NM_018102.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr20:44581130 T>A maps to NM_022095.3 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr20:25657101 G>T maps to NM_015655.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr10:38345386 G>T maps to NM_006954.1 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr10:38344972 G>T maps to NM_006954.1 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr10:38344863 A>T maps to NM_006954.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:38345148 G>A maps to NM_006954.1 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-70-6722-01A-11D-1817-08 chr10:38344908 C>A maps to NM_006954.1 Y619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr10:43088333 C>G maps to NM_006955.1 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr10:43088980 C>A maps to NM_006955.1 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr10:43088959 G>A maps to NM_006955.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:32340997 C>T maps to ENST00000375200 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:37369114 G>A maps to NM_003419.3 K461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr3:44700478 C>T maps to NM_003420.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:52468187 G>A maps to ENST00000391795 Q580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2786-01A-01D-1522-08 chr5:178489081 C>T maps to NM_014594.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr10:64136626 C>A maps to NM_199451.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr10:64159502 C>T maps to NM_014951.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr5:71752344 G>T maps to NM_152625.1 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr5:71756483 C>T maps to NM_152625.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr10:38404207 G>A maps to NM_003421.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:37118175 G>T maps to NM_032825.3 T459T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-22-1016-01A-01D-1521-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:180309644 G>A maps to NM_152520.4 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr2:180634368 C>T maps to NM_152520.4 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr3:21706422 A>T maps to NM_024697.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr6:27368914 A>T maps to NM_001076781.1 K256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:27368655 A>G maps to NM_001076781.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:99091385 G>C maps to NM_032164.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr8:28209071 C>G maps to NM_018660.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr18:32949402 G>A maps to NM_145756.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:148876625 A>T maps to NM_170686.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr18:72346026 A>T maps to NM_017757.2 K1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr23:47308215 G>T did not map to a codon.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr23:47307672 T>G did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:47308233 G>A did not map to a codon.
Sequencing variant TCGA-34-2608-01A-02D-1522-08 chr14:74390096 G>C did not map to a codon.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr19:8577340 C>A maps to NM_001146175.1 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr19:58087181 T>A maps to NM_017879.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4081-01A-01D-1458-08 chr16:49557636 G>T maps to NM_015069.2 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:49669852 G>C maps to NM_015069.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr19:9639139 T>C maps to NM_024106.1 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:21990987 A>T maps to NM_003423.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr19:21216940 A>T maps to NM_025189.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr19:21240181 A>G maps to NM_025189.3 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr19:21205609 G>T maps to NM_025189.3 G7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr10:31137766 G>A maps to NM_182755.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:11978606 G>A maps to NM_152262.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:11892025 C>T maps to NM_152355.2 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:11892258 C>T maps to NM_152355.2 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:11891125 C>T maps to NM_152355.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr19:12461558 A>G maps to NM_030824.2 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:12461929 G>A maps to NM_030824.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr19:12541211 G>A maps to NM_005815.4 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:134483068 C>T did not map to a codon.
Sequencing variant TCGA-43-3394-01A-01D-0983-08 chr23:134494172 G>T did not map to a codon.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr23:134481155 A>G did not map to a codon.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:44418133 G>C maps to NM_003425.3 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr6:57012975 C>G maps to NM_001031623.2 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr5:178391830 C>T maps to NM_182594.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2757-01A-01D-1522-08 chr5:178392041 G>T maps to NM_182594.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr19:37149213 G>A maps to NM_153257.2 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr9:109689780 G>A maps to NM_021224.4 Q1196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr9:109689123 G>T maps to NM_021224.4 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr9:109688262 G>A maps to NM_021224.4 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr9:109687002 C>G maps to NM_021224.4 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57085887 G>T maps to NM_001001668.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:57089576 G>T maps to NM_001001668.3 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57035939 C>T maps to NM_020813.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr19:50550135 G>A maps to NM_015428.1 K812K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr19:50548546 C>T maps to NM_015428.1 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6175-01A-11D-1817-08 chr19:50549916 C>T maps to NM_015428.1 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr5:121488582 C>T maps to NM_207317.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:57187651 C>T maps to NM_033273.1 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr7:57188612 G>T maps to NM_033273.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr7:57187552 A>G maps to NM_033273.1 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr7:57194379 C>A maps to NM_033273.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr7:57188464 G>T maps to NM_033273.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-1622-01A-01D-1521-08 chr7:57188388 C>A maps to NM_033273.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2726-01A-01D-1522-08 chr7:57194368 G>A maps to NM_033273.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr7:57187642 G>T maps to NM_033273.1 Y493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:30409554 G>A maps to ENST00000495929 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr9:114289896 G>A maps to NM_133464.2 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr9:95610354 G>C maps to NM_031486.1 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-6202-01A-11D-1817-08 chr10:44104701 G>T did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:20308007 T>C maps to NM_052852.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr19:20307845 G>A maps to NM_052852.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr10:48371119 C>T maps to NM_153034.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr19:11917125 A>T maps to NM_152356.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2758-01A-02D-1522-08 chr19:11917175 T>C maps to NM_152356.3 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3407-01A-01D-0983-08 chr19:21605992 G>T maps to NM_001076678.2 G178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr1:247492834 C>A maps to NM_032752.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr1:247464219 C>T maps to NM_032752.1 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr7:99227069 G>T maps to NM_145115.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr16:4802658 C>G maps to NM_021646.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr19:32844194 G>C maps to NM_014910.4 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr20:62591482 G>A maps to NM_020713.1 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6025-01A-11D-1817-08 chr20:62598348 C>A maps to NM_020713.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2744-01A-01D-0983-08 chr20:62595204 G>T maps to NM_020713.1 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr2:27603053 T>C maps to NM_144631.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr8:146033404 C>T maps to NM_213605.2 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2789-01A-01D-0983-08 chr10:97918052 A>G maps to NM_014803.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr18:22806087 C>T maps to NM_015461.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr18:22804668 G>C maps to NM_015461.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr18:22806789 T>A maps to NM_015461.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr18:22805046 G>A maps to NM_015461.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr18:22805568 C>T maps to NM_015461.2 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr19:56113997 C>T maps to NM_153219.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr19:37879572 G>T maps to NM_032453.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:52919337 C>T maps to NM_032423.2 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4601-01A-01D-1441-08 chr19:52919740 G>T maps to NM_032423.2 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:30935824 C>G maps to NM_014717.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:31039660 C>T maps to NM_014717.1 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:30934939 C>T maps to NM_014717.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:30936439 C>A maps to NM_014717.1 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:31040278 G>A maps to NM_014717.1 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:30936631 C>A maps to NM_014717.1 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:30934870 C>A maps to NM_014717.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr19:31039655 C>T maps to NM_014717.1 Q1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:30934948 C>A maps to NM_014717.1 C160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:31040371 T>A maps to NM_014717.1 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr19:30935602 C>T maps to NM_014717.1 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr19:31038892 G>A maps to NM_014717.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:31039094 C>T maps to NM_014717.1 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:58773196 G>T maps to NM_014480.2 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr19:57909796 G>T did not map to a codon.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:57910183 G>T maps to NM_001172773.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr19:58050031 G>T maps to ENST00000376233 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:58198326 C>A maps to ENST00000356715 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1076-01A-02D-1521-08 chr19:2832367 A>T maps to NM_001102651.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:2834378 C>T maps to NM_001102651.1 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:2853167 G>T maps to NM_152791.4 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:2877438 C>G maps to NM_024967.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4135-01A-01D-1352-08 chr19:7082908 A>G maps to NM_024341.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr19:8922259 C>T maps to NM_144693.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr19:9453740 G>T maps to NM_032497.1 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2771-01A-01D-0983-08 chr19:9453518 A>C maps to NM_032497.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr19:9577720 C>A maps to NM_152476.2 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr19:9578077 G>A maps to NM_152476.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr19:9578917 A>T maps to NM_152476.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5035-01A-01D-1441-08 chr19:9727721 C>T maps to NM_152289.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr19:9763922 G>C maps to NM_001130032.1 S328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2721-01A-01D-1522-08 chr19:9764311 G>C maps to NM_001130032.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr19:9764538 C>A maps to NM_001130032.1 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5234-01A-01D-1632-08 chr19:12429652 T>A maps to NM_145276.2 K396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:12638155 G>A maps to NM_144976.3 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:36673706 G>A maps to ENST00000355114 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr19:36940337 A>G maps to NM_001145343.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:37210387 A>T maps to ENST00000423498 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr19:37211128 A>G maps to ENST00000423498 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:37210999 C>T maps to ENST00000423498 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5474-01A-01D-1632-08 chr19:37904953 G>A maps to NM_152484.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:37975042 G>A maps to NM_144694.1 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr19:38055701 G>C maps to NM_016536.3 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:38056779 G>A maps to NM_016536.3 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr8:125989626 G>T maps to NM_152412.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr19:38229488 A>G maps to NM_001172690.1 G634G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr19:42583418 C>T maps to ENST00000222339 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr19:42584935 A>G maps to ENST00000222339 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:52376399 C>T maps to NM_032679.2 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:52376051 G>T maps to NM_032679.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:53014381 C>T maps to NM_001099694.1 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:53015036 C>G maps to NM_001099694.1 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:56089971 G>C maps to NM_152600.2 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr19:56090270 G>C maps to NM_152600.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr19:56895309 G>A maps to NM_144690.1 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:56935137 C>T maps to NM_001159861.1 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr19:37642520 C>A maps to ENST00000356958 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:37676856 C>A maps to NM_152279.3 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr19:37677355 C>T maps to NM_152279.3 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:58290272 C>T maps to NM_017652.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5030-01A-01D-1441-08 chr15:85327189 G>T maps to NM_014630.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr17:5086470 C>A maps to NM_032530.1 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr17:5087059 A>G maps to NM_032530.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr17:5087216 G>C maps to NM_032530.1 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr4:59996 A>T maps to NM_182524.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr4:53385 G>T did not map to a codon.
Sequencing variant TCGA-66-2791-01A-01D-0983-08 chr16:2049971 G>T maps to ENST00000431526 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:35250051 G>A maps to NM_001007248.2 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr19:53270591 A>T maps to NM_198457.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr19:53269322 G>A maps to NM_198457.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5477-01A-01D-1632-08 chr19:58489706 G>A maps to NM_025027.3 Q781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr5:123983394 G>A maps to NM_020747.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr15:64791888 A>T maps to NM_015042.1 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:52857606 G>A maps to NM_001161425.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr19:52443503 G>T maps to NM_001031721.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:52447995 C>G maps to NM_001031721.3 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:52448632 C>T maps to NM_001031721.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr19:52521330 T>C maps to NM_025040.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:52497491 C>T maps to ENST00000354939 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr19:52496579 G>A maps to ENST00000354939 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4538-01A-01D-1267-08 chr19:52633753 C>T maps to NM_178523.3 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2754-01A-01D-0983-08 chr9:116811777 C>T maps to ENST00000374126 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr9:116812084 G>T maps to ENST00000374126 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr3:40529230 C>T maps to NM_001145082.2 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr3:40571727 G>A maps to NM_001098414.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:40571742 G>A maps to NM_001098414.1 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr5:16465210 C>T maps to NM_033414.2 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr5:16465699 C>G maps to NM_033414.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr5:16451870 T>G maps to NM_033414.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr17:16526039 T>C maps to NM_020787.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr17:16527677 C>T maps to NM_020787.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5016-01A-01D-1441-08 chr19:12256216 T>C maps to ENST00000439556 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:20807956 G>A maps to NM_001076675.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr19:20828523 G>A maps to NM_001076675.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr23:47918008 A>T did not map to a codon.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr23:47920197 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:47918464 C>T did not map to a codon.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:71591281 C>T maps to NM_014497.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2756-01A-01D-1522-08 chr2:71607695 G>T did not map to a codon.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr2:71651065 G>A maps to NM_014497.3 L1474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr2:71607681 T>G maps to NM_014497.3 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr3:179050861 G>C maps to NM_016331.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr3:179051540 A>G maps to NM_016331.1 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr1:40954797 C>G maps to NM_198494.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr23:22292375 G>C did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:22291548 C>A did not map to a codon.
Sequencing variant TCGA-66-2763-01A-01D-1522-08 chr23:22291403 C>A did not map to a codon.
Sequencing variant TCGA-66-2768-01A-01D-1522-08 chr23:22292128 C>T did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:22292312 C>A did not map to a codon.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr16:31090222 C>T maps to NM_014699.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr16:31090537 C>T maps to NM_014699.3 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr16:31088352 G>A maps to NM_014699.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2794-01A-01D-1267-08 chr16:31089489 G>A maps to NM_014699.3 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr1:182025846 G>A maps to NM_001009992.1 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6560-01A-11D-1817-08 chr1:182026107 G>A maps to NM_001009992.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:88189749 C>T maps to NM_018293.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr3:88189790 C>G maps to NM_018293.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5039-01A-01D-1441-08 chr9:40772778 C>T maps to NM_033160.5 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56969569 C>T maps to ENST00000342634 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:56973715 G>A maps to ENST00000342634 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr19:56953097 C>T maps to ENST00000342634 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5472-01A-01D-1632-08 chr19:56952733 G>A maps to ENST00000342634 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2765-01A-01D-1522-08 chr19:56953172 C>T maps to ENST00000342634 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr16:31073462 C>T maps to NM_001172669.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr1:247264611 G>A maps to NM_024804.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr1:247202711 C>A did not map to a codon.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr23:46332324 C>T did not map to a codon.
Sequencing variant TCGA-21-5786-01A-01D-1632-08 chr19:22364050 T>A maps to NM_001001411.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:22364155 G>T maps to NM_001001411.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:22363000 T>C maps to NM_001001411.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4604-01A-01D-1267-08 chr19:22363756 T>C maps to NM_001001411.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:22363555 G>T maps to NM_001001411.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:22363357 A>G maps to NM_001001411.2 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5027-01A-21D-1817-08 chr19:22363342 G>T maps to NM_001001411.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr19:22362955 A>T maps to NM_001001411.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:22375844 T>G maps to NM_001001411.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:22363231 G>T maps to NM_001001411.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:53741316 G>T maps to NM_182609.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3408-01A-01D-0983-08 chr1:26688384 G>A maps to ENST00000436292 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr16:30616763 G>A maps to NM_138447.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr1:247150664 T>C maps to NM_020394.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr8:144378211 C>A maps to NM_030895.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr8:146067568 G>A maps to ENST00000446747 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr22:24086610 G>A maps to NM_021916.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-6026-01A-11D-1817-08 chr19:12058350 C>T maps to NM_144566.1 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2783-01A-01D-1267-08 chr19:12059436 G>T maps to NM_144566.1 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr19:53086016 A>C maps to NM_001172655.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr8:37556170 C>A maps to NM_025069.1 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr8:81599490 G>C maps to NM_001033723.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2713-01A-01D-1522-08 chr8:81733700 G>A maps to NM_001033723.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr8:144776411 C>G maps to NM_173831.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr19:21476636 T>A maps to NM_021269.2 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5929-01A-11D-1817-08 chr19:21477004 C>A maps to NM_021269.2 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57133812 C>T maps to NM_021216.4 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr19:57133944 G>T maps to NM_021216.4 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5240-01A-01D-1441-08 chr15:90623045 C>A maps to NM_198526.2 Y660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3415-01A-01D-0983-08 chr23:84526735 G>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:84526180 C>A did not map to a codon.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr23:84502613 G>T did not map to a codon.
Sequencing variant TCGA-22-4613-01A-01D-1441-08 chr23:84510641 G>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:84525777 G>C did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:84526675 G>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr23:84510708 C>A did not map to a codon.
Sequencing variant TCGA-60-2711-01A-01D-1522-08 chr23:84502614 C>G did not map to a codon.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr23:84502602 G>T did not map to a codon.
Sequencing variant TCGA-18-3406-01A-01D-0983-08 chr19:21299685 G>A maps to NM_182515.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr19:21299982 T>G maps to NM_182515.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:21299679 G>A maps to NM_182515.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:21300742 A>T maps to NM_182515.3 K425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr4:437771 C>A maps to NM_133474.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2724-01A-01D-1522-08 chr4:437082 A>G maps to NM_133474.2 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr22:20761086 C>T maps to NM_003426.2 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr7:149174138 C>A did not map to a codon.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr16:30545880 G>A maps to NM_023931.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr19:57955211 G>A maps to NM_001023561.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:80789460 C>T maps to NM_024702.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr17:80790023 G>A maps to NM_024702.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr17:80788545 G>A maps to NM_024702.2 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr17:80789003 C>A maps to NM_024702.2 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:3366912 A>G maps to NM_153028.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2719-01A-01D-1522-08 chr23:134427657 C>T did not map to a codon.
Sequencing variant TCGA-66-2727-01A-01D-0983-08 chr23:134421513 T>A did not map to a codon.
Sequencing variant TCGA-37-5819-01A-01D-1632-08 chr19:53959360 A>T maps to NM_001008401.3 K534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:53952763 G>C did not map to a codon.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr19:53959048 A>T maps to NM_001008401.3 K430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:12089326 G>T maps to NM_001012753.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5131-01A-01D-1441-08 chr19:12089389 C>T maps to NM_001012753.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr16:30566769 G>A maps to NM_033410.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:53905316 G>C did not map to a codon.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr15:35275458 C>T maps to NM_014106.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2782-01A-01D-1522-08 chr15:35273850 G>A maps to NM_014106.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5927-01A-11D-1817-08 chr15:90897908 C>A maps to NM_001004309.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5928-01A-11D-1817-08 chr7:150094921 C>T maps to NM_173680.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:58265934 G>A maps to NM_173632.3 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr7:149129235 C>A maps to ENST00000440594 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5232-01A-21D-1817-08 chr16:89289671 C>T maps to NM_182531.2 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr16:89293454 G>A maps to NM_182531.2 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1011-01A-01D-1521-08 chr19:40541730 C>G maps to NM_001005851.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-5897-01A-11D-1632-08 chr19:40540886 G>A maps to NM_001005851.2 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:38160680 C>T maps to NM_152605.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:38160623 T>C maps to NM_152605.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr7:148769494 G>T maps to NM_152411.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr7:148768903 C>A maps to NM_152411.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr7:148771625 A>G maps to NM_152411.3 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4583-01A-01D-1441-08 chr9:130207073 G>T maps to NM_007135.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr9:130206948 C>T maps to NM_007135.2 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3417-01A-01D-1441-08 chr19:37314232 T>C maps to NM_206894.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:35449186 G>A maps to NM_175872.4 H524H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3412-01A-01D-0983-08 chr19:35451838 G>T maps to NM_175872.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5239-01A-21D-1817-08 chr19:58806805 A>G maps to NM_021089.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr19:58805629 G>A maps to NM_021089.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4595-01A-01D-1267-08 chr3:113955260 C>A maps to NM_007136.3 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5021-01A-01D-1441-08 chr3:113955591 G>T maps to NM_007136.3 C110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr3:113955204 G>A maps to NM_007136.3 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5471-01A-01D-1632-08 chr7:127014785 C>A maps to NM_176814.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr7:127026189 T>A maps to NM_176814.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr2:185803647 C>T maps to NM_194250.1 S1175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr2:185802006 A>G maps to NM_194250.1 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr2:185800830 C>A maps to NM_194250.1 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5231-01A-21D-1817-08 chr2:185803425 T>A maps to NM_194250.1 T1101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-5236-01A-21D-1817-08 chr2:185801787 C>A maps to NM_194250.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3769-01A-01D-0983-08 chr2:185803013 C>A maps to NM_194250.1 S964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr2:185801202 C>A maps to NM_194250.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:88963588 A>T maps to NM_181646.2 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:88965076 C>T maps to NM_181646.2 I927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr7:88965830 C>T maps to NM_181646.2 R1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3410-01A-01D-0983-08 chr7:88963090 C>T maps to NM_181646.2 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4086-01A-01D-1352-08 chr7:88964012 T>C maps to NM_181646.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr7:88964053 A>G maps to NM_181646.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr7:88964015 G>T maps to NM_181646.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6143-01A-11D-1817-08 chr7:88963672 G>T maps to NM_181646.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6545-01A-11D-1817-08 chr7:88966162 A>T maps to NM_181646.2 T1289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr7:88963234 A>C maps to NM_181646.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr7:88965728 C>T maps to NM_181646.2 Q1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr7:88965208 C>T maps to NM_181646.2 G971G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4591-01A-01D-1267-08 chr23:47775903 C>G did not map to a codon.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr23:47774727 C>T did not map to a codon.
Sequencing variant TCGA-37-4133-01A-01D-1352-08 chr23:47774986 G>T did not map to a codon.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr23:47775611 G>C did not map to a codon.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr23:47774985 A>G did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:53994667 G>A maps to NM_001004301.3 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:53995064 G>T maps to NM_001004301.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr19:53995208 G>T maps to NM_001004301.3 G575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:53989884 G>C did not map to a codon.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr19:53453973 G>T maps to NM_001031665.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2600-01A-01D-1522-08 chr19:53454622 C>T maps to NM_001031665.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr19:53454511 A>G maps to NM_001031665.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr19:11833646 G>C maps to NM_001080493.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4599-01A-01D-1441-08 chr4:146823588 C>A maps to ENST00000508784 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr4:146770698 C>A maps to ENST00000508784 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3414-01A-01D-0983-08 chr13:115091161 C>A maps to NM_032436.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:37399310 C>T maps to NM_001171979.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2770-01A-01D-1522-08 chr17:33289389 C>T maps to NM_052857.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:57767366 G>A maps to NM_178457.1 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr20:57768719 C>T maps to NM_178457.1 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5489-01A-01D-1632-08 chr20:57828031 G>T did not map to a codon.
Sequencing variant TCGA-33-4547-01A-01D-1267-08 chr20:57769736 C>T maps to NM_178457.1 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-6737-01A-11D-1817-08 chr20:57768530 C>G maps to NM_178457.1 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5019-01A-01D-1817-08 chr20:57769076 G>A maps to NM_178457.1 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr20:57766526 C>A maps to NM_178457.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2734-01A-01D-0983-08 chr20:57829122 C>A maps to NM_178457.1 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:57176236 C>T maps to NM_001005850.1 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3768-01A-01D-0983-08 chr19:57175600 G>A maps to NM_001005850.1 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr14:102800976 G>A maps to NM_018335.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr14:102792674 G>A maps to NM_018335.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4582-01A-01D-1441-08 chr19:9869344 G>A maps to NM_001077624.1 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4533-01A-01D-1267-08 chr19:21133023 T>C maps to NM_003429.4 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:21132555 C>A maps to NM_003429.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2766-01A-01D-1522-08 chr19:21131616 G>A maps to NM_003429.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-3920-01A-01D-0983-08 chr7:149545451 C>T maps to NM_001099220.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1012-01A-01D-1521-08 chr19:23544807 C>A maps to NM_003430.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5485-01A-01D-1632-08 chr19:23542726 T>C maps to NM_003430.2 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr19:23544020 G>C maps to NM_003430.2 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2710-01A-01D-1522-08 chr19:23544208 G>A maps to NM_003430.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3411-01A-01D-0983-08 chr7:64863283 G>A maps to NM_152626.2 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4721-01A-01D-1441-08 chr19:20044846 C>T maps to NM_031218.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:22941186 A>T maps to ENST00000397104 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1002-01A-01D-1521-08 chr19:22940610 A>G maps to ENST00000397104 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-34-2596-01A-01D-1522-08 chr19:22940574 T>C maps to ENST00000397104 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr19:22941882 C>A did not map to a codon.
Sequencing variant TCGA-43-5668-01A-01D-1632-08 chr19:22952051 C>T maps to ENST00000397104 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr19:22940796 T>C maps to ENST00000397104 K547K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4079-01A-01D-1458-08 chr19:22941147 G>A maps to ENST00000397104 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:22941561 G>T maps to ENST00000397104 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2712-01A-01D-1522-08 chr19:22942392 A>G maps to ENST00000397104 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2723-01A-01D-1522-08 chr19:22942385 T>A maps to ENST00000397104 K130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2787-01A-01D-0983-08 chr19:22939150 G>T maps to ENST00000397104 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2795-01A-02D-0983-08 chr19:22940718 A>T maps to ENST00000397104 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-85-6561-01A-11D-1817-08 chr19:22940352 C>T maps to ENST00000397104 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4593-01A-21D-1817-08 chr20:47880002 C>T maps to NM_021035.2 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-2578-01A-01D-1522-08 chr20:47886893 G>A maps to NM_021035.2 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr22:29445638 C>T maps to NM_032173.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2777-01A-01D-1267-08 chr22:29442801 C>T maps to NM_032173.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr11:60635144 C>T maps to NM_207341.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4532-01A-01D-1267-08 chr11:60635138 A>T maps to NM_207341.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-43-6647-01A-11D-1817-08 chr16:21211168 G>C maps to NM_003460.1 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-56-6546-01A-11D-1817-08 chr16:21215488 T>C maps to NM_003460.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr1:238053839 G>T maps to NM_021186.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr1:238053450 C>A maps to NM_021186.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-39-5037-01A-01D-1441-08 chr7:50097645 G>C maps to NM_007009.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr3:102175083 G>T maps to NM_175056.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2720-01A-01D-1522-08 chr10:126631519 G>A maps to NM_017580.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr2:135965198 C>A maps to NM_032143.2 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3421-01A-01D-0983-08 chr19:58565187 C>T maps to NM_182572.3 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-5787-01A-01D-1632-08 chr19:58549347 G>T maps to NM_182572.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr19:58565154 G>A maps to NM_182572.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr16:3140291 G>A maps to NM_032805.1 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-63-5128-01A-01D-1441-08 chr16:3139745 C>T maps to NM_032805.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr19:58601295 G>A maps to NM_001145542.1 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3783-01A-01D-1267-08 chr19:58601474 C>A maps to NM_001145542.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-51-4080-01A-01D-1458-08 chr19:58596177 G>A maps to NM_001145542.1 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-1016-01A-01D-1521-08 chr15:85164478 G>A maps to NM_181877.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-4141-01A-02D-1352-08 chr15:85164139 C>A maps to NM_181877.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr1:33960552 C>A maps to NM_145238.3 S870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2742-01A-01D-0983-08 chr1:33945087 G>T maps to NM_145238.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2698-01A-01D-1522-08 chr15:43662015 C>T maps to NM_152455.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2780-01A-01D-1522-08 chr15:43662012 C>G maps to NM_152455.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2785-01A-01D-1522-08 chr15:43661910 C>G maps to NM_152455.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr19:58187555 G>T maps to NM_152677.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3419-01A-01D-0983-08 chr19:56733293 C>A maps to NM_024303.1 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1077-01A-01D-1521-08 chr19:56701293 C>A maps to NM_001080456.2 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr19:56702223 G>A maps to NM_001080456.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4566-01A-01D-1441-08 chr20:44506324 G>T maps to NM_080752.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-21-1081-01A-01D-1521-08 chr19:13928129 C>T maps to NM_023072.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-37-3789-01A-01D-0983-08 chr19:13941474 G>T maps to NM_023072.2 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5491-01A-01D-1632-08 chr1:45671860 G>T maps to NM_020883.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-33-4586-01A-01D-1441-08 chr1:45501738 C>T maps to NM_020883.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-60-2722-01A-01D-1522-08 chr1:45501722 A>G maps to NM_020883.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-4607-01A-01D-1267-08 chr11:113608371 C>T maps to NM_004724.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-22-5473-01A-01D-1632-08 chr11:113608311 G>C maps to NM_004724.2 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2773-01A-01D-1267-08 chr11:113628513 C>T maps to NM_004724.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-4083-01A-01D-1352-08 chr10:58119446 C>A did not map to a codon.
Sequencing variant TCGA-21-1070-01A-01D-1521-08 chr23:57935968 C>A did not map to a codon.
Sequencing variant TCGA-39-5024-01A-21D-1817-08 chr23:57935712 C>A did not map to a codon.
Sequencing variant TCGA-39-5031-01A-01D-1441-08 chr23:57935957 G>T did not map to a codon.
Sequencing variant TCGA-46-3765-01A-01D-0983-08 chr23:57935670 C>A did not map to a codon.
Sequencing variant TCGA-60-2708-01A-01D-1522-08 chr23:57936553 C>A did not map to a codon.
Sequencing variant TCGA-21-5782-01A-01D-1632-08 chr23:57618657 C>T did not map to a codon.
Sequencing variant TCGA-43-6770-01A-11D-1817-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-18-3416-01A-01D-0983-08 chr3:126185160 G>A maps to NM_025112.4 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2759-01A-01D-1522-08 chr1:53279332 C>T maps to NM_024646.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-5595-01A-01D-1632-08 chr7:143079461 G>A maps to NM_001010972.1 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-18-3409-01A-01D-0983-08 chr17:3966126 G>A maps to NM_015113.3 S1601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2767-01A-01D-1522-08 chr17:3919649 C>A maps to NM_015113.3 S2704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-66-2788-01A-01D-0983-08 chr1:78031387 G>A maps to NM_015534.4 Y883Y. Only missense variants will be evaluated by CHASM.
