826 NP_001070868 L216R not found in SNVbox database
2706 NP_001070868 N208S not found in SNVbox database
2945 NP_001070868 M237I not found in SNVbox database
3318 NP_001070868 E421G not found in SNVbox database
3714 NP_001070868 D574E not found in SNVbox database
3905 NP_001070868 R361Q not found in SNVbox database
4074 NP_001070868 G194V not found in SNVbox database
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr10:52573742 C>A maps to NM_138932.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr12:9254108 G>A maps to NM_000014.4 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr12:9020924 C>T maps to NM_144670.3 R1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr12:8990996 G>A maps to NM_144670.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr12:53701428 G>A maps to NM_015665.5 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr12:125621262 C>T maps to NM_023928.3 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr3:151545683 T>G maps to NM_001086.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr2:219130789 T>A maps to ENST00000444053 K255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr2:219134724 C>A maps to ENST00000444053 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr4:57220263 G>A maps to NM_181806.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1325-01A-01W-0490-10 chr9:107560699 A>G did not map to a codon.
Sequencing variant TCGA-09-1666-01A-01W-0615-10 chr2:215914347 A>T did not map to a codon.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr2:215865724 A>T maps to NM_173076.2 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr2:215823126 G>A maps to NM_173076.2 Y1997Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr7:48318489 C>T maps to NM_152701.3 Q2567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr7:48450174 C>T maps to NM_152701.3 R4043R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr7:48315556 T>G maps to NM_152701.3 T2098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr16:2329008 G>A maps to NM_001089.2 C1494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr16:2373599 C>T maps to NM_001089.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr1:94522195 G>T maps to NM_000350.2 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr1:94528846 G>A maps to NM_000350.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr1:94495003 G>T maps to NM_000350.2 P1512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr7:87170746 G>A maps to NM_000927.3 R749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr7:87144681 G>A maps to NM_000927.3 D1049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr1:229685101 G>T maps to NM_012089.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr7:87032468 C>T maps to NM_018849.2 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr7:87076385 G>C maps to NM_018849.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr23:74375964 G>A did not map to a codon.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr23:74295251 A>G did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr16:16205320 G>T maps to ENST00000399408 V997V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr16:16130331 G>A maps to ENST00000399408 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr16:16196532 T>C maps to ENST00000399408 N908N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr6:43400777 C>T maps to NM_033450.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr6:43406409 G>A maps to NM_033450.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr6:43415477 G>A maps to NM_033450.2 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr16:48230202 C>A maps to NM_032583.3 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr16:48227792 C>T maps to NM_032583.3 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr16:48264373 G>A maps to NM_032583.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr3:183639180 C>T maps to NM_005688.2 E1407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr3:183669340 G>A maps to NM_005688.2 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr16:16267248 T>G maps to NM_001171.5 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr12:22086846 G>A maps to NM_005691.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr12:21968762 G>A maps to NM_005691.2 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr12:22012549 C>T maps to NM_005691.2 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr7:150911145 G>A maps to NM_005692.3 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr7:150912710 G>C maps to NM_005692.3 Y503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr3:183910417 C>G maps to NM_018358.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr3:183905927 G>T did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr21:43710218 G>A maps to NM_004915.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr4:89042872 G>T maps to NM_004827.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr2:44051193 C>A maps to NM_022436.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr2:44073367 C>T maps to NM_022437.2 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr2:44071692 C>T maps to NM_022437.2 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr13:108882234 A>G maps to NM_032859.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr15:89694982 G>A maps to NM_152924.4 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr3:43743851 G>A maps to NM_016006.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr19:17411732 A>T maps to NM_024527.4 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr1:179076960 C>T maps to NM_007314.3 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr5:148596589 A>T maps to NM_014945.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr9:136135221 C>T did not map to a codon.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr6:26598253 C>G maps to NM_013375.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr3:38175456 G>A maps to NM_001607.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr17:35454848 T>C maps to NM_198834.1 L2212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr12:109660343 G>A maps to NM_001093.3 S1199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr12:109617850 G>T maps to NM_001093.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr12:112187148 C>T maps to NM_001136538.1 R970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr3:132350183 C>T did not map to a codon.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr1:76216134 G>A did not map to a codon.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr1:76215159 G>A maps to ENST00000370834 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr17:7125516 C>T maps to ENST00000356839 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr15:89382074 A>G maps to NM_013227.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr17:7250360 C>T maps to NM_014716.3 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr11:108012383 T>C maps to NM_000019.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr17:43213976 C>T maps to NM_001135706.1 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr1:180257596 G>A maps to NM_032360.3 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr2:220402767 G>T maps to NM_018674.4 *667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr2:220396851 T>A did not map to a codon.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr11:44075011 C>A maps to NM_001031854.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr11:44069678 G>A maps to NM_001031854.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr23:15593881 A>G did not map to a codon.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr23:15596407 G>A did not map to a codon.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr23:15585935 T>A did not map to a codon.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr19:6333532 G>A maps to NM_133492.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr14:23549130 G>A maps to NM_014977.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr9:32407427 G>A did not map to a codon.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr1:55059670 A>T maps to NM_015547.3 K144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr5:80659642 G>A maps to NM_130767.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1574-01A-01W-0615-10 chr5:80641810 C>T maps to NM_130767.2 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr23:23731272 G>C did not map to a codon.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr23:23723952 C>A did not map to a codon.
Sequencing variant TCGA-36-1580-01A-01W-0615-10 chr17:73945441 C>G did not map to a codon.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr2:272226 C>T maps to NM_007099.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr1:147126383 C>A maps to NM_016361.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr1:147131779 G>A maps to NM_016361.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr22:51183313 C>T maps to NM_001097.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr12:6749261 C>T maps to NM_032489.2 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr12:6753369 G>A maps to NM_032489.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr23:70823892 G>A did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:70828949 T>A did not map to a codon.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr23:70823744 C>T did not map to a codon.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr23:70824339 C>G did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:70823984 C>T did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr15:78471001 G>A maps to NM_015162.4 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr19:6182868 C>T maps to NM_030924.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr4:185679024 C>T maps to NM_001995.2 W611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:108912274 G>A did not map to a codon.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr23:108924289 G>T did not map to a codon.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr23:108902670 T>C did not map to a codon.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr16:20673153 T>C maps to NM_052956.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr16:20781478 C>G maps to NM_005622.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr12:7463141 C>T maps to NM_001080454.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr12:7457109 G>A maps to NM_001080454.1 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr12:81613840 A>G maps to NM_024560.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1416-01A-01W-0549-09 chr5:56777652 G>C maps to NM_001017992.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr15:35085653 G>A maps to NM_005159.4 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr7:100243918 C>A maps to NM_016188.4 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr9:111624724 C>T maps to NM_006687.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr9:111624742 G>A maps to NM_006687.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr1:18153007 G>A maps to NM_030812.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr1:18152312 C>T maps to NM_030812.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr1:236900456 T>G maps to NM_001103.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr1:236906285 G>T maps to NM_001103.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr2:98275812 A>G did not map to a codon.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr3:53911333 A>T maps to NM_022899.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:127185494 G>A did not map to a codon.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr23:127185237 C>G did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr23:127185518 C>T did not map to a codon.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr23:127185281 C>A did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:127185082 G>T did not map to a codon.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr23:127185329 A>C did not map to a codon.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr12:52377950 G>C did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr2:158399268 G>C maps to NM_145259.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr12:52307368 G>T maps to NM_001077401.1 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr10:127843849 C>T maps to NM_003474.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr10:127724747 G>T maps to NM_003474.4 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr8:39502936 T>C maps to NM_014237.2 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr5:156917400 C>A maps to ENST00000430702 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr8:39602413 T>A did not map to a codon.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr7:87563788 G>A maps to NM_021723.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr7:87762238 G>A maps to NM_021723.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr7:87760738 T>C maps to NM_021723.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr8:24208816 C>A maps to NM_014265.4 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr8:39068779 G>A maps to NM_145004.5 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr5:33881280 C>T maps to NM_030955.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr5:33683152 C>T maps to NM_030955.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr5:33615971 C>G maps to NM_030955.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr5:33643576 T>C did not map to a codon.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr5:5186162 A>G did not map to a codon.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr5:5239977 C>G maps to NM_139056.2 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr5:5235234 C>T maps to NM_139056.2 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr16:77355018 G>T maps to NM_199355.2 C748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr16:77465491 C>A maps to NM_199355.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr5:129037269 G>A maps to NM_133638.3 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr5:128977611 C>T maps to NM_133638.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr5:129019934 C>T maps to NM_133638.3 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr12:43846437 A>G maps to ENST00000389420 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr4:73154573 G>C maps to NM_014243.1 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr21:28305354 G>A maps to NM_007038.3 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr21:28305210 G>A maps to NM_007038.3 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr21:28302266 G>A maps to NM_007038.3 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr21:28315729 G>A maps to NM_007038.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr15:79069114 G>A maps to ENST00000258883 D512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr11:130284467 T>A maps to NM_007037.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr11:130289025 G>A maps to NM_007037.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr3:64644276 G>C maps to NM_182920.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr3:64601089 C>T maps to NM_182920.1 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr3:64587733 G>A maps to NM_182920.1 D1301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr3:64582541 G>A maps to NM_182920.1 G1381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr9:18504909 C>T maps to NM_001040272.4 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr9:136412307 G>T maps to ENST00000393061 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr9:136405822 G>A maps to ENST00000393061 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr15:84539698 T>C maps to NM_207517.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1558-01A-01W-0615-10 chr15:84651580 A>T maps to NM_207517.2 A1067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr21:46596482 G>A maps to NM_015833.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr5:7520993 G>A maps to NM_020546.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr5:7826917 C>T maps to NM_020546.2 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr5:7695867 C>A maps to NM_020546.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr2:25051012 G>T maps to NM_004036.3 Y730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr14:24787967 G>T maps to NM_139247.3 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1348-01A-01W-0494-09 chr3:123008729 G>A maps to NM_183357.2 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr16:4164237 G>C maps to NM_001116.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr16:4015997 G>A maps to NM_001116.3 N1280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr16:4042223 C>T maps to NM_001116.3 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr16:4016939 C>T maps to NM_001116.3 S966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr4:2928382 A>C maps to ENST00000503455 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr4:2916636 C>T maps to NM_014189.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr2:70905960 G>A maps to NM_001185054.1 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr2:70933507 C>T maps to NM_001185054.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr4:100208013 G>A maps to NM_000667.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr4:100268978 G>A maps to NM_000669.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr4:99993587 G>A maps to NM_000671.3 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr1:202911317 G>A maps to NM_015999.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr10:75984350 T>G did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr20:49518640 A>G maps to NM_181442.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr18:77896043 C>T maps to NM_014913.3 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr18:77894465 C>T maps to NM_014913.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr18:77894039 A>G maps to NM_014913.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr1:112033359 C>T maps to NM_020683.6 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr13:114107614 G>A maps to NM_138430.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:244587340 G>T maps to NM_001126.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr1:244579367 G>C maps to NM_001126.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr14:105212717 C>T maps to NM_199165.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr12:19593256 G>A maps to NM_001114176.1 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr23:147919204 C>T did not map to a codon.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr23:148049171 G>T did not map to a codon.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr23:148048555 T>C did not map to a codon.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr23:148037363 C>T did not map to a codon.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr23:147743676 A>T did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr23:147967463 T>C did not map to a codon.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr23:148044408 C>A did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr2:100175345 G>A maps to NM_001025108.1 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr5:132222025 T>G maps to NM_014423.3 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr4:74310760 C>T maps to NM_001134.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr12:58123469 T>A maps to NM_001122772.1 K837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr7:150815312 G>A maps to NM_031946.4 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr15:86813298 G>T did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr1:100346733 G>C did not map to a codon.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr2:178364437 T>A maps to NM_003659.3 Y485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr2:178301754 C>A maps to NM_003659.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr1:981233 G>T maps to NM_198576.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr9:88247911 A>T maps to ENST00000395847 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr9:88200413 T>A maps to ENST00000395847 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr9:88287522 C>T maps to ENST00000395847 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:115304581 G>A did not map to a codon.
Sequencing variant TCGA-36-1580-01A-01W-0615-10 chr23:115304184 C>A did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr5:35047955 C>G maps to NM_031900.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr5:177658436 T>C maps to NM_153373.2 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr7:129019562 C>T maps to NM_015328.3 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr1:27875239 A>G maps to NM_001029882.2 N1129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr11:62295495 G>C maps to NM_001620.1 V2131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr11:62301282 C>G maps to NM_001620.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr11:62292954 C>T maps to NM_001620.1 K2978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr14:105406646 A>C maps to NM_138420.2 P5047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr14:105413216 C>T maps to NM_138420.2 K2857K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr14:105418826 G>A maps to NM_138420.2 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr7:17378783 T>G maps to NM_001621.4 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr16:31540010 A>T maps to NM_016633.2 *103L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-04-1356-01A-01W-0492-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr23:129265758 G>T did not map to a codon.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr23:129271122 G>C did not map to a codon.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr23:129263594 C>G did not map to a codon.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr23:129281493 G>T did not map to a codon.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr22:21330810 G>T maps to NM_144704.2 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr7:6057485 G>T maps to NM_006303.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr21:45712970 G>T maps to NM_000383.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr9:130630641 T>C maps to ENST00000223836 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr13:42873736 T>C maps to NM_016248.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr6:151673287 T>G maps to NM_005100.3 T1254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr6:151669870 G>C maps to NM_005100.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr6:151674541 A>G maps to NM_005100.3 T1672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr6:151627039 T>G did not map to a codon.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr6:151672606 T>G maps to NM_005100.3 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr15:86273754 C>T maps to NM_006738.4 Q2371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr23:49958491 T>G did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr14:33015181 G>A maps to NM_004274.4 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr6:131602691 C>G maps to ENST00000431975 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr6:131490396 A>T maps to ENST00000431975 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr7:91722505 G>T maps to NM_005751.4 E3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr7:91632197 A>G maps to NM_005751.4 Q989Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr7:91712944 G>A maps to NM_005751.4 V2874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr6:109854525 T>C maps to NM_001145128.2 E1166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr9:117103865 T>G maps to NM_030767.4 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr9:117139669 C>T maps to NM_030767.4 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr1:109394764 C>T maps to NM_152763.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr7:134135630 C>T maps to NM_001628.2 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr10:5014863 C>T maps to NM_001353.5 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:19600385 C>T maps to NM_201252.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr1:19593796 G>A maps to NM_201252.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr14:105242057 C>T maps to NM_001014432.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr3:52239986 G>C maps to ENST00000441729 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr23:55042152 C>T did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:55047545 C>A did not map to a codon.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr4:74279228 C>T maps to NM_000477.5 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr3:105266315 A>G maps to NM_001627.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr9:75526945 C>T maps to NM_000689.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr9:75531967 C>T maps to NM_000689.3 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr9:75543928 C>T maps to NM_000689.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr3:125872284 A>T did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr3:125877468 C>T maps to ENST00000273450 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr12:112228251 C>G maps to NM_000690.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr17:19552331 G>T maps to NM_001031806.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr9:101980976 C>A maps to NM_033087.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr2:29754908 A>G maps to NM_004304.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr2:29445406 T>G maps to NM_004304.3 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr2:29445208 C>T did not map to a codon.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr2:73716957 C>A maps to NM_015120.4 A2623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr2:73677304 A>G maps to NM_015120.4 K1216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr17:7949990 G>A maps to NM_001141.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr17:7951804 C>T maps to NM_001141.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr4:113353246 C>T maps to NM_025144.3 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr4:113303689 C>T maps to NM_025144.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr4:113351617 G>A maps to NM_025144.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr4:113352994 G>A maps to NM_025144.3 E764E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr18:56246465 C>T maps to NM_052947.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr18:56204112 C>T maps to NM_052947.3 Q1102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr18:56203551 G>A maps to NM_052947.3 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr2:233244519 G>A maps to NM_001632.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr2:203807551 T>C maps to NM_024744.14 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr12:85680719 T>A maps to NM_006982.2 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr12:85677458 G>A maps to NM_006982.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr17:7385638 C>T maps to NM_001102614.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr12:53818631 T>G maps to NM_020547.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr1:110050739 C>T maps to NM_020703.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr12:47472365 C>T maps to NM_001143668.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:112022392 C>A did not map to a codon.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr23:112024316 T>G did not map to a codon.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr23:112021862 C>G did not map to a codon.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr7:38505848 C>T did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr7:38429467 A>G maps to NM_001635.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr3:49456461 A>G maps to NM_000481.3 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr1:104122080 G>T maps to NM_020978.3 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr1:104114356 C>T maps to ENST00000305865 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr2:112566575 T>C maps to NM_022662.2 V1260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr9:140081940 G>A maps to NM_013366.3 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr4:25417156 A>G maps to ENST00000510092 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr12:121773424 T>C maps to NM_016237.4 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1105-01A-01W-0484-10 chr14:77273000 G>A maps to NM_015305.3 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr14:77273064 T>G maps to NM_015305.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr8:108334356 C>T did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr1:178834752 G>A maps to NM_004673.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr9:129870338 G>A maps to NM_012098.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr8:41571691 G>T maps to ENST00000415018 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr8:41545725 C>T maps to ENST00000415018 Q1402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr4:114177018 G>A maps to NM_001148.4 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr10:61967868 C>T maps to NM_020987.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr10:61834065 A>T maps to NM_020987.2 P2191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr10:61967940 G>A maps to NM_020987.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr2:190571735 C>T maps to NM_144708.3 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr17:4076649 T>G maps to NM_016376.3 R1006R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr17:4145674 G>A maps to NM_016376.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr5:139903718 G>A maps to ENST00000253810 K1462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr5:139838208 G>T did not map to a codon.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr5:139909046 C>T maps to ENST00000253810 G2172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr5:139928547 C>T maps to ENST00000253810 C2596C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr11:113270727 A>T maps to NM_178510.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr19:17396545 C>T maps to NM_152363.4 C531C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr5:72857054 G>C maps to NM_023039.4 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr16:89351542 G>A maps to NM_013275.4 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr16:89371662 C>T maps to NM_013275.4 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr18:9255223 T>C maps to NM_015208.3 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr18:9255427 A>G maps to NM_015208.3 E721E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr4:73951026 G>A maps to NM_032217.3 N2366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr19:4200139 C>A maps to ENST00000262970 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr10:27389063 C>T maps to NM_014915.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr3:15778599 G>A maps to NM_015199.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr3:15749561 C>T maps to NM_015199.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr18:21229073 G>A maps to NM_173505.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr10:37451765 A>T maps to ENST00000374660 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr10:37486215 C>T maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr10:37430973 C>T maps to ENST00000374660 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr18:14782534 G>T maps to NM_001145029.1 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr5:94030920 A>G maps to NM_032290.3 E1027E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr12:52284731 G>A maps to NM_182608.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:145474032 A>G maps to NM_001039888.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr1:145474107 A>T maps to NM_001039888.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr1:145561929 C>T maps to NM_144698.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr2:197866487 C>T maps to NM_001195144.1 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr6:34985641 C>T maps to NM_015245.2 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr6:35051280 G>C did not map to a codon.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr12:5687610 G>A maps to ENST00000356134 N770N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr12:5916478 G>A maps to ENST00000356134 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr12:5708775 G>A maps to ENST00000356134 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr12:5708775 G>A maps to ENST00000356134 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr11:26681990 G>A maps to NM_031418.2 *982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr11:22294384 T>A maps to NM_213599.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:242135121 C>T maps to NM_001001891.3 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr19:17438566 G>A maps to NM_020959.2 D783D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr15:90349385 T>C maps to NM_001150.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr4:80940057 T>A maps to NM_001145794.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr4:80993642 G>A maps to NM_001145794.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr10:46135329 A>G maps to NM_001128324.1 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr10:81930612 C>A maps to NM_145869.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr15:60653145 G>T maps to NM_001002858.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr10:75138680 G>A maps to NM_004034.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr17:41001636 C>T maps to NM_009590.2 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr17:41004344 C>T maps to NM_003734.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr22:29735017 G>A maps to NM_001127.3 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr19:16314403 G>A maps to NM_001130524.1 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr23:15870597 T>A did not map to a codon.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr5:77477333 A>C maps to NM_003664.3 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr15:83331512 G>T maps to NM_004644.3 I903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr1:114438634 C>A maps to NM_006594.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr15:51204292 C>T maps to NM_007347.3 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr4:40892442 G>A maps to NM_004307.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr4:40829236 C>T did not map to a codon.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr5:139941749 G>A maps to ENST00000354402 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr5:112177304 C>G maps to NM_001127510.2 S2005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr5:112176618 A>G maps to NM_001127510.2 V1776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr5:112173864 T>C maps to NM_001127510.2 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr5:112174074 C>G maps to NM_001127510.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr19:1467802 C>T maps to NM_005883.2 P1501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr1:159558224 G>A maps to NM_001639.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1666-01A-01W-0615-10 chr3:49712670 C>A maps to ENST00000438011 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr14:20925433 G>T maps to NM_080649.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr2:68740804 C>T maps to NM_173545.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr19:36370070 C>G maps to NM_001024807.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr11:129993573 C>G maps to NM_001642.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr2:21233154 T>C maps to NM_000384.2 K2195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr2:21260034 C>G maps to NM_000384.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr2:21260913 A>G maps to NM_000384.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:21233085 G>A maps to NM_000384.2 I2218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr2:21259974 G>T maps to NM_000384.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr2:21230895 G>A maps to NM_000384.2 F2948F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr2:21233199 T>C maps to NM_000384.2 Q2180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr2:21258547 G>A maps to NM_000384.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr22:39427838 C>T maps to NM_152426.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr22:39497387 C>T maps to NM_001166003.1 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0911-01A-01W-0420-08 chr22:36661454 C>T maps to NM_145343.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr21:27484436 C>A maps to NM_000484.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr1:154296874 T>A maps to NM_080429.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr12:50344951 C>T maps to NM_000486.5 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr12:50344619 G>T maps to NM_000486.5 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr5:115336128 G>C did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr5:115298442 C>T maps to NM_173800.4 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:66937330 T>A did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:66942817 G>C did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr23:66765619 C>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:66943648 G>T did not map to a codon.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr23:47430407 C>T did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr4:36230973 C>T maps to NM_015230.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr5:141051839 G>A maps to NM_022481.5 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr5:141052462 G>A maps to NM_022481.5 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr7:127230152 G>T maps to NM_001662.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr11:47196803 G>A maps to NM_032389.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr8:68179364 T>C maps to NM_006421.3 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr14:68113450 G>T maps to NM_001172.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr6:129905236 C>G maps to NM_033515.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr10:24884682 G>C maps to NM_020824.3 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr10:24874561 C>T maps to NM_020824.3 T1552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr10:24911659 A>T did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr4:86915766 G>A maps to NM_001025616.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1348-01A-01W-0494-09 chr2:69049512 G>T maps to NM_001007231.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr2:69053235 C>T maps to NM_001007231.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1659-01B-01W-0615-10 chr5:142281603 C>T maps to NM_015071.4 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr5:142273828 G>A maps to NM_015071.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr1:161022311 G>A maps to NM_001025598.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr3:119112359 C>T maps to NM_020754.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr11:128842911 C>A maps to NM_001142685.1 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr11:128839370 G>A maps to NM_001142685.1 Q1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr23:130220566 C>A did not map to a codon.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr23:130222643 C>A did not map to a codon.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr23:130218610 G>A did not map to a codon.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr23:130218992 T>C did not map to a codon.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr23:130220599 C>T did not map to a codon.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr8:145763155 T>A maps to NM_025251.1 K855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr8:145773413 C>T maps to NM_025251.1 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:153175367 C>G did not map to a codon.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr23:153173341 T>C did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr14:32562905 A>C maps to NM_001030055.1 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr23:11160359 T>A did not map to a codon.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr23:11187695 G>A did not map to a codon.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr12:57870185 G>A maps to ENST00000393797 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr19:42409965 G>A maps to NM_199002.1 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:156926337 G>A maps to NM_198236.1 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr1:156911191 A>T maps to NM_198236.1 G1162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr11:120335956 A>T maps to NM_015313.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr11:120347424 A>G maps to NM_015313.2 E1111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr11:120350700 C>T maps to NM_015313.2 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr17:8215563 C>T maps to NM_173728.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr17:8218745 G>T maps to NM_173728.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:3389713 G>A maps to NM_014448.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:155931920 G>A maps to NM_001162383.1 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr5:149011738 G>A maps to NM_001001669.2 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr2:131785557 C>T maps to NM_015320.2 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr7:144060493 A>G maps to NM_005435.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:62898437 C>A did not map to a codon.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr23:62917092 A>T did not map to a codon.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr23:62917003 C>T did not map to a codon.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr23:62926238 C>A did not map to a codon.
Sequencing variant TCGA-59-2355-01A-01W-0799-08 chr23:62898373 C>T did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr1:27087416 C>G maps to NM_006015.4 S664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr1:27102195 C>T maps to NM_006015.4 Q1708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr12:46245722 C>A maps to NM_152641.2 R1273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr9:34622526 C>G did not map to a codon.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr14:58831428 A>T maps to NM_002892.3 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr1:235345428 C>T maps to NM_016374.5 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr1:235397795 A>C maps to NM_016374.5 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr15:72847704 G>A did not map to a codon.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr3:49012254 C>T maps to NM_006321.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr23:100243216 G>C did not map to a codon.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr23:100240795 G>T did not map to a codon.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr10:104465189 T>G maps to NM_004311.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr1:202104654 C>A did not map to a codon.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr1:202104864 T>C maps to NM_138795.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr10:28229686 C>T maps to NM_018076.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr16:31477441 T>C maps to ENST00000408912 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr2:232079713 G>C maps to ENST00000359743 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:100808008 C>T did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr23:100808743 C>T did not map to a codon.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr23:100808225 G>C did not map to a codon.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr23:100912312 A>C did not map to a codon.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr23:100911500 G>C did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:100911586 C>T did not map to a codon.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr23:100911659 G>A did not map to a codon.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr23:100912139 C>T did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:100880001 C>T did not map to a codon.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr23:100880255 C>G did not map to a codon.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr23:101858099 C>G did not map to a codon.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr23:101857910 T>C did not map to a codon.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr23:100871175 C>G did not map to a codon.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr10:124214257 C>A maps to NM_001099667.1 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr15:80800524 G>A maps to NM_014862.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr15:80767382 T>C maps to NM_014862.3 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr7:98985782 G>T maps to NM_005720.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr3:35835263 G>A maps to ENST00000458225 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr23:69496550 C>T did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr23:69489734 G>C did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:69497352 C>A did not map to a codon.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr23:69500666 T>A did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr5:78076317 G>A maps to NM_000046.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1546-01A-01W-0615-10 chr23:2861124 G>T did not map to a codon.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr23:3019220 G>A did not map to a codon.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr23:3002504 G>A did not map to a codon.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr23:3030319 C>A did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr23:3007645 A>C did not map to a codon.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr5:149677352 G>A maps to NM_001012301.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr4:114824077 G>A maps to NM_024590.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr4:114824056 C>T maps to NM_024590.3 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr4:77003470 A>T maps to NM_001130016.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1634-01A-01W-0615-10 chr4:77003059 C>T maps to NM_001130016.1 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr11:3661420 G>A maps to NM_001079536.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr11:122953913 G>A maps to NM_024769.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr8:131073022 C>G maps to NM_018482.2 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr8:131073205 T>C maps to NM_018482.2 G937G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr8:131181275 T>A maps to NM_018482.2 K262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr8:131124343 C>G maps to NM_018482.2 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr1:23760007 C>A maps to NM_017707.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr7:150878444 C>A maps to ENST00000422024 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr23:15306058 G>T did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:15306079 C>G did not map to a codon.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr23:63445177 T>C did not map to a codon.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr23:63445258 A>T did not map to a codon.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr10:5683796 C>A maps to NM_024701.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr2:53956674 G>A maps to NM_001164165.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr6:101165949 C>G did not map to a codon.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr1:155324363 T>C maps to ENST00000368346 Q2376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr7:65546869 C>T maps to NM_000048.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:1755403 C>T did not map to a codon.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr23:1546841 A>G did not map to a codon.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr23:1537001 C>G did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:97482383 G>C maps to NM_183356.3 Y488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr2:190531053 G>T maps to NM_019048.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr22:26829724 C>T maps to NM_020437.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:197070655 C>T maps to NM_018136.4 K2575K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr1:197115269 C>A did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr9:95236929 G>A maps to NM_017680.4 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr17:79974679 C>G maps to ENST00000306729 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr2:96789972 C>T maps to NM_001002036.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:177001898 G>C maps to ENST00000281881 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr1:176838104 C>T maps to ENST00000281881 Q1182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr1:176838035 C>T maps to ENST00000281881 Q1205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr20:31017223 A>G maps to ENST00000375687 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr20:31023268 C>T maps to ENST00000375687 H918H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr20:30956916 C>T maps to ENST00000375687 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr2:25990449 A>T did not map to a codon.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr2:25973248 C>T maps to NM_018263.4 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr1:1391265 A>G maps to NM_001039211.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr17:29184106 A>T maps to NM_024857.3 K924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr1:161771866 T>G maps to NM_007348.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr12:14577313 C>A maps to NM_018179.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr11:64677174 T>C maps to ENST00000421419 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr14:96795892 G>A maps to NM_018036.5 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr7:150720190 C>A maps to NM_173681.5 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr2:216200783 A>G maps to NM_004044.6 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr11:63420032 C>G maps to NM_015459.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr11:108199897 C>T maps to NM_000051.3 Q2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr15:25925359 C>T maps to NM_024490.3 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr5:160047636 G>A maps to NM_025153.2 A711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr5:160034015 C>T maps to NM_025153.2 K972K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr13:113512570 G>A maps to NM_032189.3 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr13:113485840 G>A maps to NM_032189.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr13:113536170 C>G maps to NM_032189.3 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr13:113481087 C>A maps to NM_032189.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr23:138844132 T>A did not map to a codon.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr23:138850579 G>A did not map to a codon.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr23:138869371 C>A did not map to a codon.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr23:138813815 C>A did not map to a codon.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr23:138865392 G>C did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:138901495 C>T did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr23:138908963 G>C did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr13:25265354 C>T maps to NM_001185085.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr1:17331267 C>A maps to NM_022089.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr3:193210931 C>A maps to NM_032279.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1634-01A-01W-0615-10 chr3:193125104 G>T maps to NM_032279.2 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1026-01B-01W-0484-10 chr3:193042718 C>T maps to NM_198505.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr3:193042676 G>C maps to NM_198505.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr1:160128841 G>A maps to NM_144699.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr1:160143369 G>A did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr16:28909648 G>A maps to NM_173201.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr16:28913203 C>T maps to NM_173201.3 D707D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr12:110720596 T>C maps to NM_170665.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr12:110783103 T>C maps to NM_170665.3 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr17:3831273 C>G did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr17:3831595 C>T maps to NM_174953.1 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr17:3850996 G>T maps to NM_174953.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr17:3851059 C>G maps to NM_174953.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr17:3850843 C>A maps to NM_174953.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr12:89995183 T>C maps to ENST00000428670 K1029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr3:10370703 C>A maps to NM_001001331.2 E1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr3:10417119 C>T maps to NM_001001331.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr23:152845738 G>A did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr3:130718396 T>C maps to NM_001001486.1 N841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr16:84497250 C>T maps to ENST00000416219 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr13:114307238 G>C maps to NM_000705.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr12:57038967 C>G maps to NM_001686.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr7:99056848 C>T maps to NM_004889.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr14:50792434 G>A maps to NM_001003803.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0911-01A-01W-0420-08 chr23:153662577 G>T did not map to a codon.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr23:153663712 C>A did not map to a codon.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr23:153662731 T>G did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr12:124220089 C>T maps to NM_012463.3 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr8:87162411 A>G maps to NM_152565.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr8:87111221 G>A maps to NM_152565.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr3:113497629 C>G maps to NM_001690.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr3:113517280 G>A maps to NM_001690.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr4:42576691 A>C maps to NM_006095.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr15:50264914 T>A maps to NM_024837.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr15:50223421 G>A maps to NM_024837.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr18:77063607 C>A maps to NM_198531.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr18:77063607 C>G maps to NM_198531.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr3:48502012 A>G maps to NM_130384.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr20:3578565 T>A maps to NM_139321.2 I1161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr10:116889145 T>C maps to NM_207303.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr10:117059758 T>A did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr10:117026366 A>G maps to NM_207303.2 E622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr10:117026309 C>T maps to NM_207303.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0889-01A-01W-0419-10 chr23:76777846 T>C did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr16:28847794 G>C maps to NM_148414.1 L1096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr23:13337615 T>G did not map to a codon.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr23:13337343 C>T did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr23:13337977 C>G did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr17:42275011 G>C maps to NM_020218.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr2:74754613 G>A maps to ENST00000258081 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr20:54948522 T>C maps to NM_198437.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr7:70229812 G>A maps to NM_015570.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr7:70236587 C>T maps to NM_015570.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr20:3065242 C>T maps to NM_000490.4 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr23:69459755 G>A did not map to a codon.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr23:69455987 C>T did not map to a codon.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr23:69460019 G>T did not map to a codon.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr19:41727908 C>A maps to NM_021913.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr17:79180659 G>A maps to ENST00000269392 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr3:28380106 C>G did not map to a codon.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr3:28380073 G>A maps to NM_022461.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr2:168725674 A>G maps to NM_020981.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr6:71603933 C>G maps to NM_080742.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr11:62388126 G>T maps to NM_012200.2 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr3:182988299 C>A maps to NM_032047.4 Y238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr17:81006595 T>C maps to NM_001009905.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr17:80923571 C>G maps to NM_001009905.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr17:47246243 C>T maps to NM_153446.2 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr19:41863905 G>T maps to NM_030578.3 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr21:30715061 G>T maps to NM_206866.1 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr6:90642162 A>G maps to NM_001170794.1 C830C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr6:90642152 C>A maps to NM_001170794.1 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr6:90660240 G>A maps to NM_001170794.1 Y528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr9:33255263 G>A maps to NM_004323.5 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr8:38067869 T>A maps to NM_004874.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr17:79425876 C>T maps to ENST00000436173 F1829F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr8:143570738 G>C maps to NM_001702.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr6:70040395 A>T did not map to a codon.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr6:69666081 T>A did not map to a codon.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr6:70034876 A>G maps to NM_001704.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr6:69348998 A>G maps to NM_001704.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr6:69666594 C>A maps to NM_001704.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr16:1388908 C>T maps to NM_003933.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr6:33543661 G>A maps to ENST00000360661 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr1:91178120 G>C maps to NM_020063.1 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr5:17275537 C>T maps to NM_006317.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr6:31603477 C>T maps to NM_080686.2 R1831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr6:31594905 C>G maps to NM_080686.2 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr6:31599150 A>T maps to NM_080686.2 K901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr6:31604060 G>A maps to NM_080686.2 Q1900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr6:31595939 G>T maps to NM_080686.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0717-01A-01W-0370-10 chr9:134358765 A>T maps to NM_013318.3 P1798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:171486772 T>C maps to ENST00000392078 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1633-01A-01W-0615-10 chr6:31614185 C>T maps to ENST00000404765 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr6:31669880 C>T maps to ENST00000375842 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr14:75991530 G>C maps to NM_006399.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr11:64757119 C>T maps to NM_138456.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr14:35227975 T>C maps to NM_013448.2 Q1440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr7:72891393 T>C maps to NM_032408.3 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr12:57008849 T>C maps to NM_013449.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr2:160294819 G>T maps to NM_013450.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:56530880 G>A maps to NM_031885.3 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr7:33376158 G>T maps to NM_198428.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr3:107510093 G>T maps to NM_001142568.1 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr19:45317432 G>A maps to NM_005581.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr1:156616812 C>G maps to NM_021948.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:156618390 G>A maps to NM_021948.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr7:107221264 A>T maps to NM_001008405.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr23:152981132 C>T did not map to a codon.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr20:52612475 A>G maps to NM_003657.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr20:52675233 G>T maps to NM_003657.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr3:165548008 C>A maps to NM_000055.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1494-01A-01W-0545-08 chr22:18209789 C>T maps to NM_015367.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr12:122492853 A>C maps to NM_020993.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr7:72954224 C>T maps to NM_001707.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:147092630 G>T maps to NM_004326.2 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr11:118773710 G>T maps to NM_182557.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr11:118772369 G>C maps to NM_182557.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr16:81320919 C>G maps to NM_017429.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr11:112087004 T>C maps to NM_031938.4 N526N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr23:39922070 G>A did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:39923121 C>G did not map to a codon.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr23:39932443 C>A did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr23:39933559 T>C did not map to a codon.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr23:39916573 C>A did not map to a codon.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:129149484 A>G did not map to a codon.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr23:129147147 A>T did not map to a codon.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr23:129148821 G>A did not map to a codon.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr23:129147047 C>G did not map to a codon.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr23:129149449 C>T did not map to a codon.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr23:129148635 C>T did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:129147720 G>T did not map to a codon.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr23:129156934 G>A did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr22:23596070 C>G maps to NM_004327.3 Y455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr14:96707139 C>T maps to NM_000623.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr5:70820122 T>G maps to NM_018429.2 S1915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:18234733 C>T did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr23:18234815 G>T did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr23:18221737 G>A did not map to a codon.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr23:18213447 G>C did not map to a codon.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr6:107391737 C>T maps to NM_001080450.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr6:107390066 C>T maps to NM_001080450.2 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr6:107419799 C>G maps to NM_001080450.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr10:13541892 C>T maps to ENST00000396900 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr19:12866267 C>T maps to NM_017682.2 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr23:102317853 G>C did not map to a codon.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr23:102564880 C>T did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr16:14738295 A>G maps to NM_016561.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr23:102004626 C>G did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:102004100 G>A did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr23:102005392 A>C did not map to a codon.
Sequencing variant TCGA-04-1517-01A-01W-0615-10 chr5:78379051 C>T maps to NM_017614.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr2:127818188 C>A maps to NM_139346.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr2:127827573 G>T maps to NM_139343.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr11:102220911 C>T maps to NM_001166.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr11:102195608 A>G maps to NM_182962.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr2:32693059 G>A maps to NM_016252.3 W1887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr7:43846615 C>T maps to NM_000712.3 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr8:22054898 G>A maps to NM_006129.4 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr23:50659304 C>A did not map to a codon.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr23:50659056 A>T did not map to a codon.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr20:6759300 A>G maps to NM_001200.2 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr4:79786719 T>C maps to NM_198892.1 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr4:81967252 C>T maps to NM_001201.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr4:81967024 A>G maps to NM_001201.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr4:81967138 C>T maps to NM_001201.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr6:55739402 G>T maps to NM_021073.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr20:55746158 G>A maps to NM_001719.2 H384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr1:40230370 T>C maps to NM_001720.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr7:34192866 C>A maps to NM_133468.3 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr2:203420661 G>A maps to NM_001204.6 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr10:43281117 C>G maps to NM_014753.3 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr23:15540591 A>C did not map to a codon.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr23:15548147 A>C did not map to a codon.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr9:16437048 T>C maps to NM_017637.5 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr5:172571574 C>T maps to NM_013979.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr15:59964834 C>A did not map to a codon.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr3:113002345 G>A maps to ENST00000273395 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr4:13617085 G>A maps to NM_148894.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr4:13612596 A>G maps to NM_148894.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr4:13617122 T>C maps to NM_148894.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr20:36932678 C>T maps to NM_001725.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr20:36956003 C>T maps to NM_001725.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1571-01A-01W-0615-10 chr20:36936065 G>A maps to NM_001725.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr20:31622566 A>G did not map to a codon.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr7:140449168 G>C maps to NM_004333.4 S637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr17:41226410 G>A maps to ENST00000471181 Q1560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr17:41197783 G>A maps to ENST00000471181 R1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr17:41256248 C>A maps to ENST00000471181 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr17:41256233 C>A maps to ENST00000471181 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr17:41246255 A>C maps to ENST00000471181 L431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr17:41245149 T>A maps to ENST00000471181 K800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr17:41203134 C>A did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr17:41246126 A>C maps to ENST00000471181 L474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr13:32910624 C>A maps to NM_000059.3 C711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr13:32914136 C>A maps to NM_000059.3 S1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr13:32950889 G>T maps to NM_000059.3 E2906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr23:154299901 G>A did not map to a codon.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr19:15376428 C>G maps to NM_058243.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr19:15366123 C>T maps to NM_058243.2 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr5:884085 C>A maps to NM_001009877.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr14:105684005 G>T maps to NM_001519.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr1:167889284 A>G maps to NM_001143674.1 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr3:9783743 G>T maps to NM_001003694.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr3:9786008 A>C maps to NM_001003694.1 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr6:36185694 C>T maps to NM_015695.2 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:135572548 C>G did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr19:55805587 C>A maps to NM_032430.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr19:55805402 C>T maps to NM_032430.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1666-01A-01W-0615-10 chr23:79988965 G>A did not map to a codon.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr23:79936994 G>C did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:79932615 T>A did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:79943571 C>T did not map to a codon.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr23:79945492 A>C did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:79947319 A>T did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr3:49699453 A>T maps to NM_003458.3 A3392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr3:49680333 G>T maps to NM_003458.3 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr3:49695016 G>A maps to NM_003458.3 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:55472681 G>A maps to NM_057176.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr19:17516279 C>G maps to NM_004335.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr10:93719830 C>T maps to NM_003972.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr16:3647921 G>A maps to NM_032444.2 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr16:3656511 G>C maps to NM_032444.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr16:3639411 G>C maps to NM_032444.2 A1409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:3658569 T>C maps to NM_032444.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr14:93709347 C>T maps to NM_001002860.2 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr21:18966580 G>A maps to NM_001130914.1 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr23:100608314 G>A did not map to a codon.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr23:100617577 C>G did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr23:100617666 G>A did not map to a codon.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr2:111415121 C>T did not map to a codon.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr10:115894802 T>G maps to NM_018017.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr10:115917408 C>T maps to NM_018017.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr10:98742723 C>A maps to NM_015652.2 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr10:98741356 T>C maps to NM_015652.2 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr10:124457544 T>A maps to NM_001010912.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr10:21804165 C>A maps to NM_207371.3 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr10:5790324 A>C maps to NM_017782.4 T1647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr10:5791734 A>G maps to NM_017782.4 E2117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr10:75671454 G>A maps to NM_001001791.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr10:33135313 A>G maps to ENST00000375025 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr10:33000615 C>T maps to ENST00000375025 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr10:50530958 G>A maps to NM_001135196.1 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr10:50533202 C>T maps to NM_001135196.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr10:120085706 C>A maps to NM_022063.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr10:128147615 A>C maps to NM_001004298.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr11:4594687 A>G maps to NM_144663.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr11:4594546 G>T maps to NM_144663.1 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr11:33566505 C>T maps to ENST00000389726 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr11:33565415 A>G maps to ENST00000389726 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr11:111796414 C>T maps to NM_080659.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr11:93486873 G>T maps to ENST00000354421 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr11:122830101 C>T maps to NM_024806.2 H762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr11:122774776 C>T maps to NM_024806.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr11:77553634 G>T maps to NM_024684.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr11:77580838 C>T maps to NM_024684.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr11:82625792 C>T maps to NM_145018.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr12:82872796 G>A maps to NM_032230.2 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr12:40076667 G>A maps to NM_001031748.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr12:103696329 G>A maps to NM_001099336.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr12:117158151 G>A maps to NM_024738.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr12:88391943 G>A maps to NM_152589.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr12:112621070 C>A did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr12:112681534 G>A maps to NM_001109662.2 S1388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr12:10332224 C>T maps to NM_153022.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr12:80650114 A>C did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr12:64609702 G>A maps to ENST00000311915 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr13:39600449 G>C maps to NM_025138.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2408-01A-01W-0799-08 chr13:31540435 C>T maps to NM_152325.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr14:60591864 T>A maps to ENST00000404681 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr14:81251439 T>C maps to NM_152446.3 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr14:91691161 C>T maps to NM_001102368.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr14:45373648 C>A maps to NM_001017923.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr14:58606016 G>A maps to ENST00000438670 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr14:74206316 G>T maps to NM_001043318.1 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr15:75195001 G>T maps to NM_020447.3 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr15:24921535 C>T maps to NM_018958.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr15:40684205 G>A maps to NM_033286.3 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr15:49833997 A>G maps to NM_152647.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr15:90119446 G>A maps to NM_152259.3 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr15:90168332 G>T maps to NM_152259.3 E1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr15:65899652 G>A maps to ENST00000420799 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr15:34648711 G>T maps to ENST00000438749 G825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr16:4563853 T>A did not map to a codon.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr16:4787850 C>A maps to NM_139170.2 S60S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-61-1900-01A-01W-0639-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr16:5115849 G>A maps to ENST00000350219 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr17:80373328 C>T maps to NM_175902.4 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr17:29227562 T>G maps to NM_024683.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr17:29231086 A>C maps to NM_024683.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr17:79205239 C>A maps to NM_144679.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr17:34193736 G>A maps to NM_152781.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr17:57289007 T>C maps to NM_018149.6 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr17:30658937 A>C maps to NM_022344.2 Y345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr17:5114167 T>G maps to NM_207103.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr17:36997525 C>T maps to NM_001080465.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr18:52258468 G>T maps to NM_173629.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr18:52262335 T>A did not map to a codon.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr18:30518007 A>G maps to NM_001105528.1 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr18:20878003 G>T maps to NM_032933.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr19:7570998 G>A maps to NM_198534.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr19:7571019 G>A maps to NM_198534.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr19:51301633 C>T maps to NM_199249.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr19:36255762 C>T maps to NM_001039887.2 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr19:14006339 T>G maps to ENST00000454313 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr19:51770625 G>C did not map to a codon.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr19:51768857 A>T maps to NM_173635.1 K87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr2:68270115 T>A maps to ENST00000407324 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr17:5341450 G>C maps to NM_001212.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr12:49730134 G>C maps to NM_001008223.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr13:24890278 C>T maps to NM_178540.3 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr13:24470987 G>A maps to NM_001007537.1 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr1:244747183 T>G maps to NM_001130957.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:111494209 G>C maps to NM_018372.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr1:200876998 G>T maps to NM_018265.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr1:11772022 G>T did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:185143926 C>T maps to NM_001105518.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr1:186355163 T>C maps to NM_017847.5 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr1:156264615 G>A maps to NM_144580.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr1:60466828 C>G did not map to a codon.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr1:226736748 C>G maps to ENST00000366788 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr6:31896507 G>A did not map to a codon.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr20:35425304 A>G maps to NM_080627.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr20:35444191 G>A maps to NM_080627.2 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr20:35509092 C>G maps to NM_080628.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr20:62493573 C>T maps to NM_080622.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr20:2796198 T>A maps to NM_080739.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr20:34618401 G>A maps to ENST00000373973 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr20:31644408 T>C maps to NM_182658.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr20:3298934 C>A did not map to a codon.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr20:20232313 C>T maps to ENST00000389655 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr20:20177350 G>A maps to ENST00000389655 K579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr20:1162097 G>T maps to NM_018354.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr20:742440 G>A maps to NM_033409.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr20:259878 G>T maps to NM_153269.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr21:33887205 A>G maps to NM_058187.3 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr22:45601673 C>T maps to NM_001009880.1 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr21:43319354 C>T maps to NM_015500.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:27803056 A>G maps to NM_032266.3 Q1206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr2:27801202 A>G maps to NM_032266.3 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr2:75928347 G>A maps to NM_003203.4 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr2:26647252 C>T maps to NM_145038.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr2:200820526 G>A maps to NM_024520.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr2:197672277 G>A maps to NM_213608.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr2:210888759 G>C maps to NM_152519.2 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr2:73456032 C>G maps to NM_032319.1 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr2:29296902 A>G maps to NM_001029883.1 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr2:74043137 A>G maps to NM_001080474.1 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr12:8212520 C>T maps to NM_004054.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr12:8211662 G>A maps to NM_004054.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr3:14724303 C>A maps to NM_032137.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr3:44409182 A>G maps to NM_173826.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr3:99886580 G>C did not map to a codon.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr3:11851156 C>G did not map to a codon.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr3:8669454 G>C maps to NM_015931.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr3:133647487 T>G maps to NM_025041.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr3:56667183 A>T maps to ENST00000447900 L1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr6:31963526 G>A maps to NM_007293.2 A1062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr4:113539520 C>T maps to NM_018392.4 W559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr4:170663134 G>A maps to NM_017867.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr9:123780130 C>G did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr9:123744120 C>T did not map to a codon.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr9:123751963 C>T maps to NM_001735.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr9:123739085 G>C maps to NM_001735.2 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr5:175740767 C>G maps to ENST00000443967 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr5:36217946 C>T maps to NM_001085411.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr5:36219719 T>A maps to NM_001085411.1 K208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr5:36197737 G>A maps to NM_001085411.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr5:154203152 C>T did not map to a codon.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr5:37198854 T>A maps to NM_023073.3 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr5:125971794 T>C maps to NM_207408.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr5:41154095 C>T maps to NM_001115131.1 T702T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr6:11723648 G>A maps to NM_001143948.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr6:34574604 C>A maps to NM_024294.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr6:13470446 G>C maps to NM_033069.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr6:30609968 G>A maps to ENST00000376485 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr6:47976658 C>T maps to NM_001013732.3 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr6:53989389 A>C maps to ENST00000502396 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr6:53989551 G>A maps to ENST00000502396 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2280-01A-01W-0799-08 chr6:54095651 C>T maps to ENST00000502396 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr6:54067032 T>C did not map to a codon.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr6:3723965 C>A maps to NM_183373.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr6:43477439 G>A maps to NM_001012974.1 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr6:99739652 G>A maps to NM_032511.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr6:99797092 C>G maps to NM_032511.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr6:121401918 A>T maps to ENST00000275159 *1299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr6:121613307 T>C maps to ENST00000275159 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr6:127797199 C>T maps to NM_001012279.2 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr6:127797196 C>G maps to NM_001012279.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr6:109480665 G>A did not map to a codon.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr6:110620244 G>A maps to NM_001123364.1 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr6:151775691 A>C maps to NM_024573.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr6:74072827 A>G maps to NM_001017361.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr6:31736893 G>C maps to NM_025258.2 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr6:31734089 C>T maps to NM_025258.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr6:31627260 A>T maps to NM_021184.3 L155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr6:71289269 G>T did not map to a codon.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr6:36887352 G>A did not map to a codon.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr5:40976933 C>T maps to NM_000587.2 Y719Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr5:40981516 C>T maps to NM_000587.2 R792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr7:31736585 T>C maps to NM_006658.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr7:25176193 A>G maps to NM_138811.3 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr7:99754754 G>A maps to NM_018275.3 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr7:43684998 C>G did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr7:120768470 G>C maps to NM_024913.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr7:120767265 A>T maps to NM_024913.4 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr7:120876862 A>G maps to NM_024913.4 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr7:112461966 C>T maps to NM_152556.2 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1950-01A-01W-0699-08 chr7:92164259 T>C maps to NM_032120.2 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr7:108524520 T>C maps to NM_001024607.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr1:57351811 G>C maps to NM_000562.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr8:144124642 C>G maps to NM_173687.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr8:144654355 C>G did not map to a codon.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr9:27294323 A>T maps to NM_020641.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr9:96080829 T>A maps to NM_001098808.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr9:35044782 C>T maps to NM_203299.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr9:72435914 G>A maps to NM_001010940.1 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr9:116185691 C>G maps to ENST00000451722 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr9:27548643 G>A maps to NM_018325.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr9:90500352 C>A maps to NM_178828.4 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr9:90503022 C>T maps to NM_178828.4 H1207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr1:150234555 G>A did not map to a codon.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr1:9019054 C>T maps to ENST00000413627 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr9:35674150 G>A maps to NM_001216.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr9:35679873 G>A maps to NM_001216.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr2:231683257 C>T maps to NM_001130850.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr1:227169788 G>C maps to NM_020247.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr1:227174164 C>T maps to NM_020247.4 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr22:24491949 G>A maps to NM_012295.3 G1281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr12:121093996 G>A maps to ENST00000453000 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr1:65130218 C>G maps to ENST00000371073 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr19:13341002 G>A maps to NM_023035.2 A1811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr19:13565964 G>A maps to NM_023035.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr9:140968007 G>A maps to ENST00000277549 Q1582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr12:2788716 G>A maps to NM_199460.2 A1781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr12:2613666 C>A maps to ENST00000399634 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr12:2774754 C>T maps to NM_199460.2 N1517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr3:53531456 C>T maps to NM_001128840.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr3:53753779 A>G did not map to a codon.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr1:181767516 G>T maps to ENST00000357570 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr1:181708290 C>T maps to ENST00000357570 D1207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:181745304 G>C maps to ENST00000357570 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr23:49084784 G>C did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr23:49075817 C>T did not map to a codon.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr23:49066097 G>A did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr23:49083070 C>G did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:201060857 G>A maps to NM_000069.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr1:201047050 G>A maps to NM_000069.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr3:55021778 A>T maps to NM_018398.2 R897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr3:54798362 T>A maps to NM_018398.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr2:152728961 A>T maps to NM_000726.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr16:24358109 C>A maps to NM_006539.3 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr16:24358115 G>A maps to NM_006539.3 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr17:65026912 G>A maps to NM_014405.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr19:54515403 G>A maps to NM_145814.1 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr19:54501502 C>A maps to NM_145814.1 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr19:54445450 C>T maps to NM_031896.4 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr2:27465201 C>T maps to NM_004341.3 I2043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr19:44129320 C>T maps to NM_145296.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr7:122303604 G>A maps to NM_001167940.1 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr7:122269373 G>A maps to NM_001167940.1 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr6:7373685 G>A maps to NM_001170692.1 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:71406133 T>A did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr12:54117432 C>A maps to NM_020898.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr7:93108737 G>A maps to NM_001164737.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr7:93063562 A>C did not map to a codon.
Sequencing variant TCGA-59-2355-01A-01W-0799-08 chr19:13051238 C>T maps to NM_004343.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr3:9803324 C>T maps to NM_003656.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr17:3787703 G>A maps to ENST00000381771 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0911-01A-01W-0420-08 chr3:49898958 C>T maps to NM_024046.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr3:49899764 C>T maps to NM_024046.3 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr1:7151368 T>C maps to NM_015215.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr1:6885167 C>T maps to NM_015215.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr1:7811266 T>A maps to NM_015215.2 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr17:4886183 A>T maps to NM_015099.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr11:64950666 G>A maps to NM_005186.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:241534124 A>G maps to NM_023083.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr2:241534672 G>A maps to NM_023083.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr6:44145088 C>T maps to NM_007058.3 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:110495618 A>T did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr23:110491920 G>A did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr23:110494209 C>T did not map to a codon.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr12:30906457 C>T maps to NM_001002259.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr22:37893154 G>A maps to NM_014550.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr7:2968266 G>A maps to NM_032415.4 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr17:78178060 C>T maps to NM_024110.2 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr17:78169021 C>A maps to NM_024110.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr17:78172296 C>T maps to NM_024110.2 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr5:40854091 A>T maps to NM_032587.3 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr13:111287050 C>T maps to NM_018210.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr11:3038503 T>A maps to NM_001014437.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr23:41446233 C>A did not map to a codon.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr23:41530716 C>G did not map to a codon.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr23:41390349 G>A did not map to a codon.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr23:41646435 G>T did not map to a codon.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr2:202070638 C>T maps to NM_032977.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr11:104819341 C>T maps to NM_001225.3 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr6:90572021 G>A maps to NM_012115.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr20:55033484 G>A maps to NM_020356.3 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr20:55033505 C>T maps to NM_020356.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr11:34470830 G>A maps to NM_001752.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr11:65788336 G>A maps to NM_053054.3 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr11:65793838 G>A maps to NM_053054.3 N4N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr15:43924548 C>T maps to NM_172095.1 W470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2016-01A-01W-0722-08 chr1:26527919 G>A maps to NM_198137.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr10:74135574 C>G maps to NM_006077.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr11:119148470 T>C maps to NM_005188.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr3:105438962 C>T maps to NM_170662.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr3:105397359 T>G maps to NM_170662.3 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:107389400 C>T maps to NM_024814.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr7:107398981 C>T maps to NM_024814.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr22:39530036 G>T maps to NM_175709.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr22:39064130 G>A maps to NM_015373.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr1:52824928 T>G maps to NM_032449.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr4:15518282 A>T maps to NM_001080522.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr4:15539712 G>A maps to NM_001080522.2 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr2:219892422 A>C maps to NM_194302.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr2:219878016 G>A maps to NM_194302.2 I1307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr5:114607080 A>G maps to NM_001040440.2 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr19:48801336 G>A maps to NM_144577.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr23:48921455 G>T did not map to a codon.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr19:33424369 C>T maps to NM_032816.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr7:23682718 G>A maps to NM_138771.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr7:31617735 C>T maps to NM_194300.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr7:31594113 G>A maps to NM_194300.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr7:31682912 C>T maps to NM_194300.2 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr7:92905559 A>G maps to NM_017667.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1728-01A-01W-0699-08 chr7:92970855 T>C maps to NM_017667.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr2:179720256 C>T maps to NM_173648.3 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr2:179732788 G>T maps to NM_173648.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr2:179702416 G>A maps to NM_173648.3 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr17:16610837 C>T maps to NM_014695.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr4:24839786 A>C maps to NM_001130726.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr11:124857708 C>G maps to NM_025004.2 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr11:124862562 C>T maps to NM_025004.2 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr22:30766772 C>G maps to NM_001017437.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr19:11462590 C>T maps to ENST00000427879 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr15:74623037 G>A maps to ENST00000321288 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr11:27360368 T>A maps to NM_030771.1 *374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr3:49294666 T>C maps to NM_178173.3 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr3:180377523 C>A maps to NM_181426.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr17:78061472 C>T maps to NM_017950.2 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr12:119961527 C>G maps to NM_178499.3 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr12:123282747 G>A did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr12:120518689 G>C did not map to a codon.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr12:120436404 G>A maps to NM_207311.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr11:93104409 C>T maps to NM_181645.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr11:93103252 G>A maps to NM_181645.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr3:49200747 C>T maps to NM_022903.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr11:32636228 T>G maps to NM_001008391.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr1:100613447 A>C did not map to a codon.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr12:549793 T>C maps to NM_032358.3 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr19:46915368 G>A maps to NM_032040.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr19:46915878 G>A maps to NM_032040.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr19:46915440 C>T maps to NM_032040.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr11:118886092 A>T maps to NM_198489.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr2:56611480 A>T maps to NM_001080433.1 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr11:60617761 G>A maps to NM_024098.3 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr11:64108209 G>T maps to NM_032251.5 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr14:91772240 C>G maps to NM_001080414.2 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr2:118703103 C>A did not map to a codon.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr5:169025559 T>G maps to NM_017785.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr17:32612889 G>T maps to NM_002986.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0717-01A-01W-0370-10 chr13:37015328 T>A maps to NM_003914.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0889-01A-01W-0419-10 chr13:37015328 T>A maps to NM_003914.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr23:50053115 G>A did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:50053208 T>A did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr23:50051867 G>T did not map to a codon.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr23:50037980 G>A did not map to a codon.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr23:50052250 C>T did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:50090708 A>G did not map to a codon.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr15:43478057 G>A maps to NM_012142.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr15:43478385 G>A maps to NM_012142.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1416-01A-01W-0549-09 chr4:78087043 C>T maps to NM_004354.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr5:86700746 C>T maps to NM_001239.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr3:156866152 C>T maps to NM_020307.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr1:1322690 G>T maps to NM_030937.4 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr1:1334551 C>T maps to NM_030937.4 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr12:49087925 A>C maps to NM_001240.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr17:40832614 A>G maps to NM_016602.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr3:46399719 C>T maps to NM_001123041.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1574-01A-01W-0615-10 chr3:45943062 C>T maps to NM_031200.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr3:46449635 C>T maps to NM_001130910.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr4:139964379 A>C maps to NM_012118.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr2:62099657 C>T maps to NM_006430.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr1:117552470 G>A did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr6:74517955 A>C maps to NM_133493.3 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr6:74517951 T>G maps to NM_133493.3 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr12:7586045 A>G maps to ENST00000416109 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr12:7531633 G>A maps to ENST00000416109 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr12:7522196 G>A maps to ENST00000416109 G1275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr5:66480367 A>G maps to NM_005582.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr1:158263247 A>C maps to NM_001765.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr1:158152680 C>T maps to NM_001766.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr3:112647780 G>A maps to NM_138806.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr2:71062876 C>T maps to NM_015717.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr19:35828817 G>A maps to NM_001771.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:160808239 C>T did not map to a codon.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr17:72470704 G>T maps to NM_007261.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr2:160636684 C>T maps to NM_001198759.1 A1741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr7:80303417 T>C maps to NM_001127444.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr11:118211201 G>A maps to NM_000732.4 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr19:45912179 G>A maps to ENST00000423698 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr11:118220582 A>T maps to NM_000073.2 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr11:60889152 C>A maps to NM_014207.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr19:42383135 C>T maps to NM_001783.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr19:14516747 C>T maps to NM_078481.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr23:149938797 C>T did not map to a codon.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:149938815 C>T did not map to a codon.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr15:43021764 C>T did not map to a codon.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr9:99266067 G>A maps to NM_033331.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr17:45221246 A>G did not map to a codon.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr1:227261713 C>G did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr1:227222459 C>T maps to ENST00000366766 Q1124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr14:103410774 A>C maps to NM_006035.3 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr6:44364162 A>G maps to NM_001253.2 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr17:38447466 A>C maps to NM_001254.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr5:24488056 C>T maps to NM_006727.3 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr5:24535260 C>T maps to NM_006727.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1428-01A-01W-0549-09 chr5:21975434 G>A maps to NM_004061.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr8:95206874 A>T maps to NM_001144663.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr8:95188825 G>A maps to NM_001144663.1 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr5:19838996 C>T maps to NM_004934.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr5:19483572 A>T maps to NM_004934.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr5:19520789 T>A maps to NM_004934.3 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr20:44841654 C>T maps to NM_021248.1 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr10:73562831 G>T maps to ENST00000398860 E2559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr20:58567483 C>T maps to NM_177980.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2436-01A-01D-1526-09 chr20:58570918 C>T maps to NM_177980.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr20:58562615 T>C maps to NM_177980.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr16:68716323 C>T maps to NM_001793.4 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr20:60499505 C>T maps to NM_001794.2 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr20:60427937 C>T maps to NM_001794.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr16:61851492 C>A maps to NM_001796.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr16:61689506 G>T maps to NM_001796.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr16:61687586 G>A maps to NM_001796.2 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr5:26988428 G>A maps to NM_016279.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr5:26881571 C>T maps to NM_016279.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr5:26915873 C>T maps to NM_016279.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr5:26988416 T>C maps to NM_016279.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr10:85972941 G>A maps to NM_033100.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr7:105655651 C>G maps to NM_152750.4 Y440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr10:62539960 G>A did not map to a codon.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr17:37627172 C>G maps to NM_016507.2 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr17:37627888 C>T maps to NM_016507.2 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr17:37649050 G>A maps to NM_016507.2 W719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr7:40127930 G>C did not map to a codon.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr7:40102475 G>T maps to NM_003718.4 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr23:47086092 T>C did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr17:30815159 C>T maps to NM_003885.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr20:31960504 T>A did not map to a codon.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr9:123234044 G>A maps to NM_018249.4 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr9:123199626 G>A maps to NM_018249.4 Q1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2095-01A-01W-0722-08 chr9:123199657 C>G maps to NM_018249.4 V1290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr7:92300798 G>A maps to NM_001145306.1 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr14:50805739 G>A maps to ENST00000356146 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr23:18668701 C>A did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr11:125875869 A>C maps to ENST00000392693 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr17:15510907 A>G maps to ENST00000455584 N728N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr6:31084482 A>C maps to NM_001264.4 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr5:149562370 C>T maps to NM_001804.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr23:72667226 G>A did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr16:80654772 C>T maps to NM_152342.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr19:51981791 C>T maps to NM_001080405.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr19:45016137 T>C did not map to a codon.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr19:42265289 G>A maps to NM_002483.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr19:42260658 A>G maps to NM_002483.4 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1328-01A-01W-0492-08 chr19:42187882 C>T maps to NM_006890.3 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr19:43093707 G>A maps to NM_001816.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr22:18022252 C>T maps to ENST00000400579 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr9:135939855 T>C maps to NM_001807.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr1:15792584 C>T maps to ENST00000375924 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr1:22313136 G>A maps to NM_007352.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr1:151681509 C>T maps to NM_007185.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr22:46787569 G>A maps to NM_014246.1 C2036C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr1:109795085 G>A maps to NM_001408.2 K795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr3:48697376 C>A maps to NM_001407.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr3:48680317 C>T did not map to a codon.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr4:104055001 G>A maps to NM_001813.2 S2190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr4:104065687 A>G maps to NM_001813.2 L1649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr4:104035656 A>G maps to NM_001813.2 L2499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr4:104104013 G>A maps to NM_001813.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr1:214813301 C>T maps to NM_016343.3 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr1:214795473 A>G maps to NM_016343.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr1:214815578 C>T maps to NM_016343.3 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr13:25487016 G>A maps to NM_018451.3 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr16:81066241 G>T maps to NM_001100625.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr9:95142142 T>A did not map to a codon.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr9:123931941 T>C maps to NM_007018.4 L2042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr9:123877462 T>C maps to NM_007018.4 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr5:122724241 T>C maps to NM_153223.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr11:117280418 C>A maps to NM_014956.4 V1278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr11:117251327 A>G did not map to a codon.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr1:243328395 G>A maps to NM_014812.2 R956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr18:13124738 A>G maps to NM_032142.3 R2528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr20:34096009 C>G maps to NM_007186.3 T2299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr20:34089715 C>T maps to NM_007186.3 L1315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr12:88465165 A>G maps to NM_025114.3 D1972D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr1:180061939 G>T maps to NM_014810.4 E2234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr1:180080187 G>A maps to NM_014810.4 L3082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr3:134256055 A>T maps to NM_025180.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr3:138213918 C>T did not map to a codon.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr9:80881398 C>T maps to NM_001098802.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr3:101476584 C>T maps to ENST00000327230 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr2:182521670 C>T maps to NM_001030311.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr16:55857571 C>A maps to NM_001025195.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr16:55880594 C>G did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr18:580773 G>A maps to NM_004066.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr6:31919722 C>T maps to ENST00000437789 H1239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr1:196716244 G>A maps to NM_000186.3 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr1:196695951 C>A maps to NM_000186.3 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr1:196799735 G>A maps to NM_002113.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr1:196871731 G>A maps to NM_006684.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr23:47489233 C>T did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr1:151508329 G>A maps to NM_020770.2 E1051E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr15:57810601 A>T maps to NM_032866.3 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr2:27324964 C>T maps to ENST00000404694 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr17:48545481 C>G maps to NM_001267.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr10:50827772 G>A maps to NM_020549.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr10:75541895 G>A maps to NM_203298.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr5:98207754 C>T maps to NM_001270.2 K1287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:146767110 G>A did not map to a codon.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr1:146756123 T>C maps to NM_004284.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr15:93499687 G>C did not map to a codon.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr17:7813860 C>T maps to NM_001005271.2 S1961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr17:7812540 C>G maps to NM_001005271.2 P1884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr12:6710172 A>G maps to ENST00000309577 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr1:6170035 C>T maps to NM_015557.2 A1799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr20:40049693 G>A maps to NM_032221.3 Q1861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr20:40111971 T>C maps to NM_032221.3 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0927-01A-02W-0419-10 chr20:40112055 C>T maps to NM_032221.3 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr20:40081474 G>A maps to NM_032221.3 D1076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr20:40042020 C>G maps to NM_032221.3 L2358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr8:61743044 T>G maps to NM_017780.2 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr8:61773614 A>G maps to NM_017780.2 K2587K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr8:61736433 C>T maps to NM_017780.2 A1079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr8:61750654 A>G maps to NM_017780.2 K1458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr8:61750673 C>T maps to NM_017780.2 R1465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr8:61654395 G>A maps to NM_017780.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr14:21870225 C>A maps to NM_001170629.1 E1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr16:53289529 A>T maps to ENST00000219084 K1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1950-01A-01W-0699-08 chr16:53301838 G>T maps to ENST00000219084 G1506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr22:29083974 C>A did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr20:5904367 C>T maps to NM_001819.2 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr1:111861830 C>G maps to NM_201653.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr1:111861299 G>A maps to NM_201653.2 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:85233819 T>A did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr23:85236775 A>T did not map to a codon.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr1:241798261 C>A maps to NM_001821.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr1:241798043 G>T maps to NM_001821.3 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr3:87294928 A>G maps to NM_014043.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr9:33267861 G>A maps to NM_016410.5 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr7:29438003 C>T maps to NM_004067.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr7:29440167 C>T maps to NM_004067.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr8:141521678 C>A maps to NM_017444.4 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr8:141521636 G>A maps to NM_017444.4 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr23:109931918 C>G did not map to a codon.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr1:240072214 A>G maps to NM_000740.2 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr1:240070819 C>T maps to NM_000740.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr2:175618345 G>A maps to NM_001039523.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr2:175619075 C>T maps to NM_001039523.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr8:42611053 C>A maps to NM_004198.3 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr17:7358629 C>T maps to NM_000747.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr17:7358670 G>A maps to NM_000747.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr8:42587043 C>T maps to NM_000749.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr2:101014520 G>T maps to NM_004854.3 C92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr12:105151232 C>T maps to NM_018413.5 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr10:125798161 C>T maps to NM_015892.3 W353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr3:142840773 G>A maps to NM_004267.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr10:101978482 G>A maps to NM_001278.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr19:42795130 C>A maps to NM_015125.3 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr19:42798379 C>T maps to NM_015125.3 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr14:24775660 G>A maps to NM_014430.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr15:65499321 C>A maps to NM_003613.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr12:120313966 C>T maps to ENST00000392521 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr12:120210660 T>C maps to ENST00000392521 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr12:106633422 C>A maps to NM_006825.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr12:106641287 G>T maps to NM_006825.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr11:46818490 C>T did not map to a codon.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr3:33686306 G>A maps to ENST00000359576 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr1:86913414 A>G maps to NM_006536.5 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr1:87031501 C>T maps to ENST00000263723 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr7:143029908 G>A maps to NM_000083.2 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr23:10166091 C>A did not map to a codon.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr23:10153169 T>A did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:49856791 G>T did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr23:49850697 T>A did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:49854819 C>A did not map to a codon.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr23:49851436 G>A did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr16:1507736 G>A maps to ENST00000382745 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1571-01A-01W-0615-10 chr16:1515270 G>A maps to ENST00000382745 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr1:16359721 A>C maps to NM_004070.3 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr1:16378238 C>T maps to NM_000085.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr21:31538577 C>A maps to NM_012131.2 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr3:137742516 C>A maps to NM_016369.3 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr3:137717847 C>A maps to NM_001002026.2 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr23:106171624 C>A did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr17:7164188 C>A maps to NM_001185022.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr3:98235670 G>C maps to NM_001040182.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr14:38724321 G>C maps to NM_175060.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr14:38723817 A>G maps to NM_175060.1 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr16:11065058 A>G maps to ENST00000409790 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr16:69985382 G>A maps to NM_182619.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr16:74452175 G>A maps to NM_001011880.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr16:70208294 G>A maps to NM_173619.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr12:8671626 T>C maps to NM_080387.4 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr6:31704065 T>C maps to NM_001288.4 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr23:154528096 C>T did not map to a codon.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr12:122821265 C>A maps to ENST00000302528 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr12:122838998 C>T did not map to a codon.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr12:122825323 A>G maps to ENST00000302528 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr12:122839859 C>G did not map to a codon.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr7:73752997 C>T maps to NM_003388.4 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr2:201724422 C>G maps to NM_001162407.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr5:178050267 T>C maps to NM_020666.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:28499047 C>T maps to NM_000086.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr13:77570167 C>T maps to NM_006493.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr11:57427142 T>A maps to NM_006831.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr5:1335184 G>A maps to NM_030782.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr12:7301636 C>T maps to NM_014718.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr22:19175513 C>A maps to NM_007098.3 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr22:19241625 G>A maps to NM_007098.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1950-01A-01W-0699-08 chr22:19183894 C>T maps to NM_007098.3 W1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr16:3573214 C>T maps to NM_015041.1 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr18:645001 C>G maps to NM_199167.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr6:123319035 C>T maps to NM_001010852.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr12:22214387 T>G did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr12:108686409 G>C maps to NM_001142344.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr5:79030431 G>A maps to NM_153610.3 P1948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr5:79034472 G>C maps to NM_153610.3 L3295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr5:79033852 G>T maps to NM_153610.3 E3089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr5:79029372 A>T maps to NM_153610.3 A1595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr5:79033752 A>G maps to NM_153610.3 K3055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr8:88364007 C>T maps to NM_173538.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr4:47945299 G>C maps to NM_001142564.1 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:150906977 T>C did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr23:150909360 T>A did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr23:150912848 C>A did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:99013681 C>T maps to NM_001298.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2095-01A-01W-0722-08 chr2:99012778 C>T maps to NM_001298.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr11:6265371 C>T maps to NM_001037329.2 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr16:57951378 G>A maps to NM_001297.4 N653N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:57921794 C>T maps to NM_001297.4 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:26515324 C>T maps to ENST00000374253 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0801-01A-01W-0370-10 chr6:154727784 C>T maps to NM_173515.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr1:95363309 G>A maps to NM_001839.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr10:104679499 C>T maps to NM_017649.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr2:97498310 C>G maps to NM_017623.4 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr19:54655964 C>T maps to NM_014516.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr6:42905540 C>T maps to NM_006586.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr6:88853949 G>A maps to NM_016083.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr1:24201882 G>A maps to NM_001841.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr9:34557626 G>T maps to NM_147164.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr9:34556273 G>T maps to NM_147164.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr9:34564606 C>A maps to NM_147164.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr12:41316222 C>T maps to NM_001843.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr3:3067876 G>A maps to NM_175607.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr3:1339576 G>A maps to NM_014461.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr17:40842769 G>A maps to NM_003632.2 W623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr7:146536933 C>A maps to NM_014141.5 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr7:146829350 T>C maps to NM_014141.5 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr16:76569457 A>G maps to NM_033401.3 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr2:125175106 C>T maps to NM_130773.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr2:124999867 G>A maps to NM_130773.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr2:125261999 A>C maps to NM_130773.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr2:125671732 C>A maps to NM_130773.2 Y1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr2:125521566 C>T maps to NM_130773.2 N791N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr7:51261213 T>C maps to ENST00000395542 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr2:165600306 T>C maps to ENST00000392717 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr1:230820960 A>G maps to NM_007357.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr7:106876939 A>T maps to NM_006348.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr16:23436106 G>A maps to NM_153603.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr17:55019485 T>A did not map to a codon.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr1:103404626 C>T maps to NM_080629.2 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr1:103491076 C>T maps to NM_080629.2 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1545-01A-01W-0615-10 chr6:33132637 G>A maps to NM_080680.2 D1618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr6:75838021 A>G maps to ENST00000322507 N2110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1105-01A-01W-0484-10 chr6:75855865 G>A maps to ENST00000322507 I1504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr6:75892995 G>C maps to ENST00000322507 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr6:75833986 T>C maps to ENST00000322507 K2236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr10:71678072 G>A maps to ENST00000356340 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr10:71654429 G>C did not map to a codon.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr8:121237329 G>T maps to NM_021110.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr8:121309823 C>A maps to NM_021110.1 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr8:121259882 G>A maps to NM_021110.1 V837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr9:101767280 G>A maps to NM_001855.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr9:101829165 G>T maps to NM_001855.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr1:32149595 G>A maps to NM_001856.3 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr1:32146504 C>T did not map to a codon.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr1:32163509 G>C maps to NM_001856.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr1:32157225 G>T maps to NM_001856.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1109-01A-01W-0484-10 chr10:105800874 C>T maps to NM_000494.3 G883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr10:105798221 C>T maps to NM_000494.3 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr7:94040247 C>T maps to NM_000089.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr8:139815147 G>A maps to NM_152888.1 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr8:139688815 C>A maps to NM_152888.1 G1045G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr8:139890116 G>A maps to NM_152888.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr8:139618623 C>T maps to NM_152888.1 P1368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr5:177674550 G>A maps to ENST00000390654 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr9:117054447 G>T maps to NM_032888.2 G1514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr9:116973263 C>T maps to NM_032888.2 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr2:189863011 T>C maps to NM_000090.3 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr2:189866315 G>A did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr13:110804760 A>T maps to NM_001845.4 C1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr13:111138035 A>G maps to NM_001846.2 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr2:227914783 C>A maps to ENST00000396625 G1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr2:227942760 T>C maps to ENST00000396625 K612K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr2:227872073 G>T maps to ENST00000396625 I1680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr23:107923910 T>G did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr23:107939570 G>A did not map to a codon.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr23:107930858 A>C did not map to a codon.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr23:107930809 C>T did not map to a codon.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr23:107683416 G>A did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:107923972 G>C did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:107924177 G>C did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:107783014 A>C did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr23:107406236 T>C did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr23:107431204 G>T did not map to a codon.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr23:107417826 G>T did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:107404857 C>A did not map to a codon.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr23:107554055 T>A did not map to a codon.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr23:107462958 A>T did not map to a codon.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr23:107403783 C>T did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:107402841 G>A did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr23:107403873 C>T did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr9:137659190 A>T maps to NM_000093.3 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr9:137582923 T>G maps to NM_000093.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr9:137716495 G>A maps to NM_000093.3 T1583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr2:189899803 G>C maps to NM_000393.3 A1397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1586-01A-02W-0633-09 chr2:189901350 T>C maps to NM_000393.3 R1368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr2:189904244 A>C maps to NM_000393.3 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr19:10071134 C>T maps to NM_015719.3 T1730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr19:10104339 A>C maps to NM_015719.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr19:10090668 C>A did not map to a codon.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr21:47549212 A>T maps to NM_058174.2 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr2:238274339 C>A did not map to a codon.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr2:238285463 T>C maps to NM_004369.3 P1007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr2:238243269 T>G maps to NM_004369.3 T3076T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr2:238303598 C>A maps to NM_004369.3 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr2:238280957 C>A maps to NM_004369.3 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:238305436 G>A maps to NM_004369.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr3:130159637 G>A maps to ENST00000312481 K2152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr3:130300561 T>A maps to NM_001102608.1 T1235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr3:130368273 C>T maps to NM_001102608.1 A1867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr3:48629184 C>T maps to NM_000094.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr3:48625775 C>T maps to NM_000094.3 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr1:40771847 G>A maps to NM_001852.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr1:40777210 C>A maps to NM_001852.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr3:15497415 G>A maps to NM_005677.3 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr5:115428327 C>T maps to NM_016144.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr22:19951092 G>A maps to NM_001135162.1 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr1:160293227 G>T maps to NM_001098398.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr11:14498515 G>C maps to NM_001144061.1 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1634-01A-01W-0615-10 chr8:67974105 C>A maps to NM_006837.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr12:6838450 G>A maps to NM_001164093.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr2:237998542 A>G maps to NM_006710.4 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1365-01A-01W-0490-10 chr4:84188771 G>A maps to NM_015697.7 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr12:120941828 C>A maps to NM_032314.3 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr15:69011493 C>A maps to NM_006091.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr16:4463378 T>A maps to NM_024535.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr20:30226829 A>C maps to NM_032609.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr3:148930322 A>G maps to NM_000096.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr7:130023568 C>T maps to NM_001868.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr7:129929520 C>G maps to NM_001869.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr3:148601469 G>C maps to NM_001870.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr7:130002340 G>A maps to NM_080385.4 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr8:68340285 C>T maps to NM_020361.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr19:17091433 G>A maps to ENST00000443236 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr17:28772783 C>A maps to NM_001304.4 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr5:175306957 C>T maps to NM_001008220.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr3:194062381 C>G maps to NM_001080513.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr3:194062468 T>C maps to NM_001080513.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr20:34219654 G>A maps to NM_003915.5 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr14:24545434 C>T maps to NM_006032.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr16:89643969 G>C maps to NM_014427.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1586-01A-02W-0633-09 chr3:9767735 G>A did not map to a codon.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr2:207804353 T>C maps to NM_173077.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:207804355 G>A maps to NM_173077.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr2:211523336 C>A maps to NM_001122633.1 T1233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr2:211441114 C>G maps to NM_001122633.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1416-01A-01W-0549-09 chr2:211460243 C>T maps to NM_001122633.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr2:211521298 G>A maps to NM_001122633.1 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr2:211441214 G>A did not map to a codon.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr14:92600682 G>A maps to NM_017437.1 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr7:29111386 A>C did not map to a codon.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr23:88008811 C>T did not map to a codon.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr23:88008467 A>T did not map to a codon.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr23:88009030 C>T did not map to a codon.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr20:2778885 G>A maps to NM_019609.4 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr10:125514209 G>A maps to NM_198148.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr1:207785130 C>A maps to NM_000651.4 L2135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:207741238 C>A maps to NM_000651.4 P1341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr1:207881608 G>C did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr1:207640106 G>T maps to NM_001006658.2 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr12:94072615 G>T maps to NM_003805.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr12:94072639 C>G maps to NM_003805.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr9:126133039 C>T maps to NM_173689.5 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr11:46332691 G>A maps to ENST00000288400 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr11:46337936 G>T did not map to a codon.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr7:137569783 C>T maps to NM_194071.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr7:137613043 G>C maps to NM_194071.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr19:4157239 A>G maps to NM_032607.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr16:3786809 C>G maps to NM_004380.2 V1467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr16:3790511 G>A maps to NM_004380.2 R1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr16:3789577 C>A did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr7:30695300 C>T maps to ENST00000348438 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr2:36744581 C>T maps to NM_016441.2 C701C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr6:49704163 C>T maps to NM_001190986.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr8:75898260 A>C maps to NM_031461.5 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr8:75941626 C>A maps to NM_031461.5 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr20:6017786 C>T maps to NM_019095.4 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr4:5843062 G>A maps to NM_001014809.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr20:20031248 C>T maps to NM_016652.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr1:17295771 G>A maps to NM_014675.3 R1746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr7:87027958 A>G maps to NM_001143935.1 *641W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr10:99667898 G>A maps to NM_018058.4 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr19:18886578 G>A maps to NM_001098482.1 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr1:153921791 T>A maps to NM_181715.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr1:153925750 G>A maps to NM_181715.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr12:107393836 T>C maps to NM_004075.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr17:27577315 C>T maps to NM_005208.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr21:34974578 C>A maps to ENST00000416217 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr23:151909158 G>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr1:115282493 G>A maps to NM_001130523.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr5:149435639 G>A maps to NM_005211.3 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:1407744 G>A did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr23:1419503 G>T did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:1409296 G>A did not map to a codon.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr23:1404672 C>T did not map to a codon.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr8:2820090 G>A maps to NM_033225.5 S3175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr8:2832111 G>A maps to NM_033225.5 N2867N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr8:3076921 T>C maps to NM_033225.5 E1509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr8:2964059 T>A maps to NM_033225.5 P2313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr8:2910122 G>A maps to NM_033225.5 T2507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr1:33998803 C>T maps to ENST00000373381 T3299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr1:34554714 G>A maps to ENST00000373381 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr1:34128622 C>T maps to ENST00000373381 E1334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr1:34076683 G>A maps to ENST00000373381 S2060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr1:34076710 G>T maps to ENST00000373381 S2051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr1:33990500 G>A maps to ENST00000373381 G3419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr8:113504880 G>T maps to NM_198123.1 G1705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr8:113277814 G>T maps to NM_198123.1 I3171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr8:113418908 T>A maps to NM_198123.1 R1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr8:113347627 A>C maps to NM_198123.1 T2365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr8:113276039 A>T maps to NM_198123.1 A3230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr4:70826668 T>G maps to NM_001891.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr22:38696912 C>A maps to NM_001894.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr6:31637141 C>G maps to ENST00000375885 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr15:75969141 G>A maps to NM_001897.4 F1906F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr3:39185370 A>T maps to NM_033027.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr3:39185034 G>A maps to NM_033027.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr3:39185735 C>T maps to NM_033027.3 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr20:23731338 A>G maps to NM_001898.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr20:23615889 C>A did not map to a codon.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr11:65780320 C>T maps to NM_001323.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr23:153881763 C>T did not map to a codon.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr7:143882722 T>C maps to NM_198495.2 D709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr1:85036343 T>C maps to NM_004388.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr2:219269105 C>T maps to NM_021198.1 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr2:219266329 C>T maps to NM_021198.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr5:138145785 C>T maps to ENST00000355078 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr10:68381521 G>A maps to NM_013266.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr10:68940272 T>C maps to NM_013266.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr10:68940232 G>A maps to NM_013266.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr3:41278076 A>G did not map to a codon.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr3:41266886 C>T maps to NM_001904.3 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr1:9910817 C>T maps to ENST00000361853 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr20:36470758 T>C maps to NM_030877.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr11:57573403 C>T maps to NM_001085458.1 H591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr5:11397166 T>C maps to NM_001332.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:16701312 C>G did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr23:16696533 C>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:16688748 T>C did not map to a codon.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr23:16635354 C>G did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr16:75258619 C>T maps to NM_001906.4 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr11:88042467 G>T maps to NM_001814.4 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr1:206328778 A>T maps to ENST00000361052 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr1:206320306 C>T maps to ENST00000361052 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr14:25043624 C>T maps to NM_001911.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr14:25043612 C>G maps to NM_001911.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr4:156864416 C>T did not map to a codon.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr7:117431497 C>T maps to NM_033427.2 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr7:117424413 T>G maps to NM_033427.2 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1471-01A-01W-0551-08 chr7:117432607 G>A maps to NM_033427.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr19:7990282 C>G maps to NM_206833.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr10:16982055 C>A maps to NM_001081.3 T1841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr10:17142217 A>G maps to NM_001081.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr10:35328010 C>T did not map to a codon.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr10:35317782 T>C maps to NM_001198778.1 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:119694127 G>A did not map to a codon.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr6:43008014 C>T maps to NM_001168370.1 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr6:43154023 G>A maps to ENST00000354495 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr7:101840496 T>G maps to ENST00000360264 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr7:101833139 G>A maps to ENST00000360264 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr7:101882769 C>T maps to ENST00000360264 Q1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr10:124598698 G>A maps to NM_022034.4 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr17:36971121 G>A maps to NM_017748.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr4:78528990 T>G did not map to a codon.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr2:219029136 G>A maps to NM_000634.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr23:70836444 C>A did not map to a codon.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr23:70837302 C>T did not map to a codon.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:70836958 A>T did not map to a codon.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr23:70836821 C>T did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr11:118764861 C>G maps to NM_001716.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr23:30578014 C>T did not map to a codon.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr23:35985796 C>T did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr23:35985744 C>A did not map to a codon.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr23:19983771 T>C did not map to a codon.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr23:40496387 C>G did not map to a codon.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr23:106466000 T>C did not map to a codon.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr23:105868475 C>T did not map to a codon.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr23:105855951 C>T did not map to a codon.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr23:36162689 G>A did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr23:70323948 C>A did not map to a codon.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr23:37663163 A>G did not map to a codon.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr7:25163376 C>T maps to NM_018947.5 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr15:22958294 G>A maps to NM_014608.2 W646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr15:22991214 C>G maps to NM_014608.2 G968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr15:22955195 C>T maps to NM_014608.2 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr23:83128901 A>C did not map to a codon.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr23:83128242 A>T did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:83128000 G>A did not map to a codon.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr23:83128697 A>T did not map to a codon.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr23:83128419 C>A did not map to a codon.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr15:74636160 A>G maps to NM_000781.2 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr8:143999034 C>T maps to NM_000498.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr15:51504726 T>C maps to NM_031226.2 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr15:75042234 G>A maps to NM_000761.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr15:75042399 C>A maps to NM_000761.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr2:72371320 G>T maps to NM_019885.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr19:41352953 G>T maps to NM_000762.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr19:41518369 C>T maps to NM_000767.4 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr19:41509967 G>C maps to NM_000767.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr10:96731979 G>A maps to NM_000771.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr19:41627881 C>T maps to NM_000774.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr11:14902269 G>A maps to NM_024514.4 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr7:99361630 G>A maps to NM_017460.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr7:99457613 G>T did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr7:99459330 G>C maps to NM_022820.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr7:99314834 C>T maps to ENST00000292414 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr1:47279974 C>G maps to NM_001099772.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:47264866 G>T maps to NM_001099772.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr19:15794392 G>A maps to NM_023944.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr19:15756569 G>A maps to NM_000896.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr19:15760866 C>T maps to NM_000896.2 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr19:15756581 C>T maps to NM_000896.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr8:59404923 G>A maps to NM_000780.3 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr3:42917232 G>A maps to NM_004391.2 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr23:77528368 G>C did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:77529002 C>A did not map to a codon.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr23:77528319 T>C did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr22:37695332 C>T maps to NM_013385.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr4:5018905 C>A maps to NM_018659.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr5:39383070 C>T maps to NM_001343.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr5:39383169 G>A maps to NM_001343.2 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr9:124521254 C>T maps to ENST00000408936 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:86071102 G>T did not map to a codon.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr23:86069729 A>T did not map to a codon.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr23:85994759 C>A did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr23:85950138 T>A did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr11:61511045 G>A maps to NM_006133.2 E738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr7:6456310 G>A maps to NM_139179.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr12:109281279 C>T maps to NM_001917.4 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr1:155698873 C>T maps to NM_004632.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr1:155701155 G>T maps to NM_004632.3 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr9:90312051 C>T maps to NM_004938.2 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr2:136741008 T>G maps to NM_001349.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr6:33287495 G>T maps to NM_001350.4 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr6:33288656 G>A maps to NM_001350.4 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr7:87537202 C>T maps to NM_006716.3 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr9:136507528 G>A maps to NM_000787.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr5:176899145 G>A maps to NM_080881.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr23:125685994 G>T did not map to a codon.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr23:125298655 C>A did not map to a codon.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr23:125298738 C>T did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:125299586 G>A did not map to a codon.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr23:125298897 C>T did not map to a codon.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr23:125299721 C>A did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr19:14070607 A>G maps to NM_138353.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr8:88885116 G>A maps to NM_152418.3 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr8:88886088 G>A maps to NM_152418.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr14:69521947 G>T maps to NM_003861.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1416-01A-01W-0549-09 chr17:61662658 C>T maps to NM_005828.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr23:27998164 C>T did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:27998265 C>T did not map to a codon.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr23:27998771 C>G did not map to a codon.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr6:117853526 G>T maps to ENST00000338728 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr18:50734185 C>T maps to NM_005215.3 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr18:50832016 C>T maps to NM_005215.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr18:50912488 C>T maps to NM_005215.3 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr18:50912509 T>A did not map to a codon.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr4:155305579 G>A maps to NM_017639.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr4:71891558 G>A maps to ENST00000504952 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr4:71889368 A>G maps to ENST00000504952 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr13:36686116 C>T maps to NM_004734.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr10:14950523 G>A maps to NM_001033855.1 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr10:14981853 G>T maps to NM_001033855.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr12:91558417 G>T maps to NM_133503.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr12:2061827 C>T maps to NM_152640.3 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr1:155014238 G>A maps to NM_152494.3 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr1:155005606 G>A maps to NM_144622.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr2:74596554 G>T maps to NM_004082.4 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:74593455 G>C maps to NM_004082.4 S892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr16:20873512 A>G maps to NM_173475.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr23:110644254 C>T did not map to a codon.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr23:110653403 C>T did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr19:17425169 G>T maps to NM_024050.5 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr19:17425148 C>T maps to NM_024050.5 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr11:61083825 T>C maps to NM_001923.3 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr7:50596923 C>T maps to NM_000790.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr7:50611678 G>A maps to NM_000790.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr14:53570518 C>T maps to NM_001160148.1 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr8:38095662 G>T maps to NM_001164232.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr6:110729541 T>C maps to NM_003649.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr1:20981952 G>A maps to NM_005216.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:162722918 C>T maps to NM_006182.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr1:162745440 G>C did not map to a codon.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr22:38883956 C>T maps to NM_001098504.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr22:38881981 T>C maps to NM_001098504.1 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr10:70723143 G>A maps to NM_004728.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr14:94521518 G>A maps to NM_020414.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr23:134706754 G>T did not map to a codon.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr23:134706895 C>T did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:41206138 G>C did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:41206146 A>C did not map to a codon.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr6:74104867 C>T maps to NM_018665.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr10:70695820 C>T maps to NM_024045.1 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr23:23019107 G>A did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr4:169206559 A>G maps to NM_017631.5 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr8:91013758 C>T maps to NM_001359.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr6:49989592 C>T did not map to a codon.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr6:49986695 C>T maps to NM_001037497.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr20:29960709 C>T maps to NM_054112.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr20:29960790 C>T maps to NM_054112.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr20:210246 C>A maps to NM_080831.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr9:126146014 C>T maps to NM_020946.1 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr9:126392755 C>G did not map to a codon.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr1:197481074 C>T did not map to a codon.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr19:6467576 G>A maps to NM_024898.2 Q782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr8:142186754 G>A maps to NM_014957.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr22:32253445 G>A maps to NM_001136029.1 Q1048Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr22:32162609 C>T maps to NM_001136029.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr8:121061813 G>T did not map to a codon.
Sequencing variant TCGA-36-2540-01A-01D-1526-09 chr8:124027737 G>A maps to NM_024295.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr22:24179303 G>A maps to NM_001135751.1 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr7:24784260 G>A maps to NM_001127453.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr23:69421816 G>T did not map to a codon.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr23:69424949 T>G did not map to a codon.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr12:56334430 G>A maps to NM_201554.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr7:14647108 T>C maps to NM_004080.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr7:14378176 G>A maps to NM_004080.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr7:14741332 C>T maps to NM_004080.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr2:234297006 G>T maps to NM_152879.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr7:137271923 C>A maps to NM_004717.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr7:137269993 G>A maps to NM_004717.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr23:50213384 G>A did not map to a codon.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr23:50122708 C>G did not map to a codon.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr23:50213219 G>T did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:50144108 G>C did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr14:24108192 G>C maps to NM_182908.4 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr23:2326806 C>T did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr23:2161117 G>C did not map to a codon.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr4:24543632 G>A maps to NM_001358.2 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr5:54581180 A>G maps to NM_019030.2 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr3:47888806 G>A maps to NM_138615.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr10:127526956 C>G did not map to a codon.
Sequencing variant TCGA-25-1328-01A-01W-0492-08 chr17:5347809 G>T maps to ENST00000457531 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr19:47861377 G>C did not map to a codon.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr16:72137912 G>A maps to NM_014003.3 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr2:39085967 T>A maps to NM_198963.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr17:41571122 G>T maps to NM_004941.1 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:182845603 A>G maps to NM_001357.4 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr12:122701098 C>T maps to NM_019887.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr5:140956438 C>G did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr23:96396766 T>C did not map to a codon.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr23:96502830 A>T did not map to a codon.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr23:96185749 A>T did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr23:96204030 G>T did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr23:96013248 G>T did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr13:60545192 A>C maps to NM_001042517.1 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr20:61512108 G>A maps to NM_033081.2 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0717-01A-01W-0370-10 chr12:51097920 A>T did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr12:51069110 G>C did not map to a codon.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr12:51092137 A>G maps to NM_173602.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr12:51092122 A>T maps to NM_173602.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr10:468809 G>A maps to NM_014974.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr10:436257 G>C maps to NM_014974.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr10:415515 C>T maps to NM_014974.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr13:73345226 G>A maps to NM_014953.3 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr15:66618703 T>G did not map to a codon.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr15:66625340 G>C did not map to a codon.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr15:40661534 C>A maps to NM_033510.1 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr15:40659779 G>T maps to NM_033510.1 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr4:107845720 A>T maps to NM_014421.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr11:12023929 A>G maps to ENST00000450094 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr8:42231698 A>G maps to NM_014420.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr8:13251202 C>T did not map to a codon.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr8:12960304 C>T maps to NM_182643.2 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr3:38139129 T>A did not map to a codon.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr3:38139094 G>A maps to NM_007335.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr23:69719791 G>A did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr23:69670153 C>T did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:69671760 C>G did not map to a codon.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr10:79576318 T>G maps to NM_004747.3 R1339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr10:79569427 G>T maps to NM_004747.3 S1508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr10:79576406 G>A maps to NM_004747.3 I1309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr18:3879420 G>A maps to NM_004746.2 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr8:1497659 C>T maps to ENST00000357934 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr8:1649523 C>T maps to ENST00000357934 R982R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr1:35370750 C>T maps to NM_001080418.1 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr1:35370972 G>A maps to NM_001080418.1 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr20:35128067 G>A maps to ENST00000339266 E696E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr14:101200563 C>T maps to NM_003836.5 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr14:101201220 C>T maps to NM_003836.5 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr6:170597384 A>G maps to NM_005618.3 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1574-01A-01W-0615-10 chr2:172966864 A>G did not map to a codon.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr7:96639146 A>T maps to NM_005222.3 K224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr10:124377809 C>T maps to ENST00000368915 L1723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr10:124361449 A>C maps to ENST00000368915 R1161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr1:46977889 G>A maps to NM_147192.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr22:38964240 C>T maps to NM_007068.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1365-01A-01W-0490-10 chr23:31140011 C>A did not map to a codon.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr23:32583899 G>T did not map to a codon.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr23:31893419 T>A did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr23:32380909 C>A did not map to a codon.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr23:32663205 C>T did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:32382761 C>G did not map to a codon.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr23:32583977 T>C did not map to a codon.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr23:31165529 G>T did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:31165498 G>T did not map to a codon.
Sequencing variant TCGA-25-1627-01A-01W-0615-10 chr23:31497166 C>T did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr23:32536136 T>C did not map to a codon.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr23:31187670 T>C did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:31144779 G>T did not map to a codon.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr9:894143 T>A maps to NM_021951.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr9:990674 C>A maps to NM_021240.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0968-01A-01W-0484-10 chr5:118576152 T>C maps to NM_005509.4 N2876N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr15:51773447 C>T maps to NM_001174116.1 W1952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr15:51829846 T>G maps to NM_001174116.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr15:51829059 C>A did not map to a codon.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr15:51742415 C>T maps to NM_001174116.1 T2938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr10:70229847 C>G maps to NM_001080449.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr3:52388950 C>T maps to ENST00000273600 D1191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr3:52357822 G>A did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr12:124297817 T>A maps to NM_207437.3 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr7:21784162 A>G maps to NM_003777.3 K2761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr7:21609826 T>C maps to NM_003777.3 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr7:21640502 A>G maps to NM_003777.3 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr3:57509541 A>G maps to NM_178504.4 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr17:76487590 G>A maps to ENST00000389840 I2187I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-29-1761-01A-01W-0633-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr17:7660423 C>G maps to NM_020877.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr17:7691401 A>C did not map to a codon.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr16:21063049 A>G maps to NM_017539.1 Y1393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr16:21132166 G>T maps to NM_017539.1 Y531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr16:20974701 C>A maps to NM_017539.1 E3502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr5:13754366 T>C maps to NM_001369.2 K3500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr5:13769113 C>A maps to NM_001369.2 L3284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr5:13864742 A>T maps to NM_001369.2 C1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr5:13859657 G>C maps to NM_001369.2 S1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr5:13923469 G>A maps to NM_001369.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr2:196737141 G>T maps to NM_018897.2 G2155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr2:196822074 A>T maps to NM_018897.2 S996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr6:38877310 T>C maps to ENST00000327475 R3165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr6:38942235 G>C maps to ENST00000327475 L4243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr6:38775493 C>G did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr6:38862479 A>T maps to ENST00000327475 K2851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr17:11648367 G>T maps to NM_001372.3 L2122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr17:11835359 G>A maps to NM_001372.3 T4045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr17:11672605 C>T maps to NM_001372.3 N2504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr17:11757663 C>A maps to NM_001372.3 P3284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr17:72285861 C>T maps to NM_023036.4 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr2:234652220 G>C maps to NM_001001394.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr7:157177651 G>A maps to NM_058246.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr7:157178321 G>A maps to NM_005494.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr5:138773236 G>A maps to NM_152686.3 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr12:49743188 C>T maps to NM_024902.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr12:49745257 C>T maps to NM_024902.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr20:62559772 C>T maps to NM_025219.2 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr1:65855050 G>T maps to ENST00000371069 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:38027203 G>A maps to NM_003462.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr3:58183603 C>T maps to NM_004944.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1626-01A-01W-0615-10 chr19:12986911 T>G maps to NM_001375.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr9:131008773 G>A maps to ENST00000372923 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr1:171956926 C>T maps to ENST00000359070 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr10:101716492 G>T maps to ENST00000342239 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr10:101715847 G>A maps to ENST00000342239 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr20:31376727 C>G maps to NM_006892.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr20:44430076 G>T maps to NM_052951.2 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr10:128797684 C>T maps to ENST00000398025 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr23:117809929 G>T did not map to a codon.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr23:117699973 A>G did not map to a codon.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr23:117706330 G>C did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:117702116 G>A did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr5:169435499 G>T did not map to a codon.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr3:51274941 C>T maps to NM_004947.4 R675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr3:51399376 G>C maps to NM_004947.4 L1698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr7:111430593 C>T maps to ENST00000428084 Q1078Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr7:111418329 A>T did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr8:25261088 G>T maps to NM_024940.6 E1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr19:11353932 C>A did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr19:11312612 G>A maps to ENST00000319867 H1882H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr19:11354519 G>A maps to ENST00000319867 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr9:372250 A>T maps to NM_203447.3 K692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr5:176936637 C>T maps to NM_024872.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr20:53171518 T>C maps to NM_018431.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr20:53205044 G>A maps to NM_018431.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr9:131847013 G>C maps to NM_020438.4 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr6:30919552 T>A maps to NM_080870.3 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr1:44437735 T>C maps to NM_001384.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr1:101456176 C>T maps to NM_015958.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr1:155112491 C>T maps to NM_018973.3 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr2:116510873 G>A did not map to a codon.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr2:116510800 A>T maps to NM_020868.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr2:116548887 C>G maps to NM_020868.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr11:66272240 T>G maps to NM_005700.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr2:162891748 G>A maps to NM_001935.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr2:162865111 A>G maps to NM_001935.3 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr7:154561238 C>T maps to NM_130797.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr15:65759461 C>A maps to NM_197960.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr3:109026936 C>T maps to NM_138815.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr19:32973052 G>A maps to NM_001172774.1 E686E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr1:98015253 T>G maps to NM_000110.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr1:98015113 A>T did not map to a codon.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr1:98165100 T>C maps to NM_000110.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr1:98039474 G>T maps to NM_000110.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr5:146777312 C>T maps to NM_001197294.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr2:27121399 C>G maps to NM_020134.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr2:27150300 G>A did not map to a codon.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr12:102315001 C>A maps to NM_018370.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:111661424 A>G did not map to a codon.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr4:9783718 G>A maps to NM_000798.4 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr17:18003899 C>A maps to NM_001388.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr23:100493998 C>T did not map to a codon.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr23:100510223 C>T did not map to a codon.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr23:100503564 C>T did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:100506032 A>G did not map to a codon.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr18:28666672 T>A maps to ENST00000438199 K283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr18:28662380 T>C maps to ENST00000438199 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr18:28605881 C>A did not map to a codon.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr21:41719663 G>A maps to NM_001389.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr21:41559850 C>A maps to NM_001389.3 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr21:41414565 A>G maps to NM_001389.3 S1806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr11:117302343 G>T maps to NM_020693.2 R1820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr6:116747990 G>T did not map to a codon.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr18:65181473 A>G maps to NM_032160.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr18:29121186 C>T maps to NM_001943.3 C637C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr18:29046616 C>T maps to NM_001944.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr18:29027851 C>A maps to NM_001944.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr18:29052245 G>C did not map to a codon.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr18:28986205 G>A maps to NM_001134453.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr20:35399276 T>G maps to NM_001145315.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr20:35396412 C>A maps to NM_001145315.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr6:7559456 A>G did not map to a codon.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr6:7583701 C>T maps to NM_004415.2 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr6:56499679 A>T maps to ENST00000361203 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr6:56504508 C>T maps to ENST00000361203 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr6:56481862 C>T maps to ENST00000281662 T2698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr6:56482018 G>T maps to ENST00000281662 V2646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr6:56480742 G>A maps to ENST00000281662 L3072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr6:56399918 C>A did not map to a codon.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr6:56481862 C>T maps to ENST00000281662 T2698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr6:56483869 C>T maps to ENST00000281662 A2218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr20:17581544 T>C maps to NM_006870.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr20:18576814 G>A maps to NM_080820.4 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr2:25678314 C>A maps to NM_021907.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr12:58000984 G>A maps to NM_178502.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr3:122288592 C>T maps to NM_138287.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr15:45444640 C>G maps to NM_175940.1 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr15:45448042 T>A maps to NM_175940.1 Y1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr15:45442896 C>T maps to NM_175940.1 I962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr15:45434296 T>C maps to NM_175940.1 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr15:45398833 G>A maps to NM_014080.4 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr15:45410235 C>T maps to NM_144565.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr10:76797755 G>A maps to NM_001003892.1 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr10:76803576 G>A maps to NM_001003892.1 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr10:76863774 C>T maps to ENST00000356369 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr12:12630090 A>G maps to NM_030640.2 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr2:96810589 G>T maps to NM_004418.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr23:44703897 G>C did not map to a codon.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr1:167095720 G>C maps to NM_001080426.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr1:167096824 C>A maps to NM_001080426.1 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr1:167095051 C>T maps to NM_001080426.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr8:29203022 G>A maps to NM_057158.2 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr12:89743204 T>C maps to NM_001946.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr23:152915086 C>T did not map to a codon.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr23:152915580 A>T did not map to a codon.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr23:152915599 A>T did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr19:57669773 A>G maps to NM_001012729.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr14:102492938 T>A maps to NM_001376.4 L2889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr14:102449374 A>G maps to NM_001376.4 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr14:102489218 T>A did not map to a codon.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr14:102461588 T>C maps to NM_001376.4 Y1172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr7:95442611 G>T maps to NM_004411.4 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr11:103075605 C>T maps to NM_001080463.1 F2789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr11:103070168 A>G maps to NM_001080463.1 G2684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr11:103153792 C>T maps to NM_001080463.1 S3630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr2:44010663 G>A maps to NM_001193464.1 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr19:40321330 G>A maps to NM_004714.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr19:40319197 G>A maps to NM_004714.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr12:68051679 G>A maps to NM_006482.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr2:71827972 G>T did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr2:71801344 G>A maps to NM_001130987.1 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr15:55722918 A>T maps to NM_130810.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr13:96277049 A>T maps to NM_198968.2 L315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr1:23836446 C>A maps to NM_004091.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr8:86121469 A>T maps to ENST00000256117 K238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr8:110573096 G>T maps to ENST00000276658 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr5:158524047 G>A maps to NM_024007.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr3:73111513 A>G maps to NM_018029.3 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr23:48382319 C>T did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:48382288 G>A did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr13:50235196 C>T maps to NM_032565.3 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr3:183975498 C>T maps to NM_014693.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr1:150483553 A>G maps to ENST00000369049 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr9:95277071 G>A maps to NM_001393.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr9:95264808 G>C maps to NM_001393.3 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:68836335 C>A did not map to a codon.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr23:68836276 T>G did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:69249372 A>T did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:69253372 G>A did not map to a codon.
Sequencing variant TCGA-24-1546-01A-01W-0615-10 chr3:5249830 C>T maps to NM_014674.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr20:57896086 T>C maps to NM_207034.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr12:93192685 T>C maps to NM_003566.3 K983K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr6:74229210 C>T maps to NM_001402.5 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr20:62119707 G>A maps to NM_001958.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr16:22278031 C>G maps to NM_013302.3 Y533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr3:128060191 G>T maps to NM_021937.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr12:3768783 G>T maps to NM_001144958.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2408-01A-01W-0799-08 chr17:28417567 C>A maps to NM_198529.3 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr22:43995976 G>A maps to NM_022785.3 Q950*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-13-0887-01A-01W-0421-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr2:56145356 T>A maps to NM_001039349.1 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr11:65635352 C>T maps to NM_016938.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr23:44120528 C>T did not map to a codon.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr23:44037779 G>T did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:68059566 G>A did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr17:7611765 G>C maps to NM_001406.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr8:133015517 G>A maps to NM_015137.3 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr17:42929827 C>A maps to NM_004247.3 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:13635854 C>G did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr9:139566725 G>A maps to NM_201446.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr5:38438522 C>T maps to ENST00000354891 C810C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr7:55273279 G>A maps to NM_005228.3 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr10:64573740 G>C maps to NM_001136178.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr2:63101663 T>C maps to NM_015252.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr2:63223824 A>T maps to NM_015252.3 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr11:64627569 G>A maps to NM_006795.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr15:42245975 G>A maps to NM_139265.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr3:184910745 C>G maps to NM_001966.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr3:184910607 C>T maps to NM_001966.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr9:140707939 G>C maps to NM_024757.4 V1046V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2095-01A-01W-0722-08 chr23:20156741 T>G did not map to a codon.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr2:88857411 G>A maps to NM_004836.5 R1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr12:124106398 G>A maps to NM_001414.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2355-01A-01W-0799-08 chr14:75475851 G>A maps to NM_014239.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr1:45341322 G>C maps to NM_020365.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1325-01A-01W-0490-10 chr3:183860378 C>T maps to NM_003907.2 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr3:183860026 G>C maps to NM_003907.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1569-01A-01W-0615-10 chr23:24086169 A>T did not map to a codon.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr11:32608571 T>G maps to NM_006360.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr17:7481743 T>C maps to NM_001416.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr3:184042724 G>T maps to NM_001194947.1 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr3:184039625 C>T maps to NM_001194947.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr3:184041296 A>G maps to NM_001194947.1 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:21191171 C>A maps to NM_001198801.1 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr1:21220077 G>A maps to NM_001198801.1 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr9:23692734 T>A maps to ENST00000359598 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr4:139980193 T>C maps to ENST00000379550 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:129203383 G>A did not map to a codon.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr22:37770641 C>A maps to NM_052906.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr23:47500735 C>G did not map to a codon.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:47498651 C>A did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:47497542 C>T did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr23:47497527 C>A did not map to a codon.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr7:37298835 T>A maps to NM_014800.9 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr7:37253053 G>A maps to NM_014800.9 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr16:67233261 C>T maps to NM_024712.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr2:85617886 G>A maps to NM_001135023.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr7:73474509 G>A maps to ENST00000358929 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr7:73456944 G>C maps to ENST00000358929 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr6:11010982 C>T maps to NM_017770.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr10:103988237 C>T maps to NM_152310.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr5:60060123 C>T maps to NM_024930.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr17:48453532 G>A maps to NM_001166131.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr7:101188709 C>G maps to ENST00000397927 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr20:39990363 G>C maps to NM_052846.1 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1635-01A-01W-0615-10 chr14:100341315 G>A maps to NM_001008707.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr19:46116929 C>T did not map to a codon.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr2:42522281 T>A maps to NM_019063.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr14:89205265 T>C maps to ENST00000380664 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr14:89129374 C>T maps to ENST00000380664 E1166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr16:10626767 G>C maps to NM_001424.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr19:6926552 G>A maps to ENST00000381407 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr19:6937604 C>A maps to ENST00000381407 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr19:14758091 A>G maps to NM_032571.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr19:14757990 A>C did not map to a codon.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr19:14774263 C>T maps to NM_032571.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr1:225702311 T>G maps to ENST00000284563 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr9:130592100 C>T maps to NM_001114753.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr1:8924017 G>A maps to NM_001428.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr1:8926470 G>A maps to NM_001428.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr12:7027205 C>T maps to NM_001975.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr17:4860151 G>A maps to NM_053013.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr18:688605 G>C maps to ENST00000319815 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr23:129762010 A>C did not map to a codon.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr23:129771384 C>A did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:129822874 A>G did not map to a codon.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr23:129801582 G>A did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr6:132211632 C>T maps to NM_006208.2 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr8:120633757 G>T maps to NM_006209.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr6:131995407 G>A maps to NM_005021.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr6:132047341 T>C did not map to a codon.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr6:132047337 T>C maps to NM_005021.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr6:46107814 T>C maps to NM_014936.4 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr6:46133124 C>A maps to NM_021572.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr22:40283671 G>A maps to NM_152512.3 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr22:40257811 T>A maps to NM_152512.3 K184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr10:97624619 T>C did not map to a codon.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr10:97599530 C>T maps to NM_001098175.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1576-01A-01W-0615-10 chr10:97599540 C>T maps to NM_001098175.1 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr3:40457426 G>T maps to NM_001248.2 G232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1659-01B-01W-0615-10 chr8:23305376 G>A maps to NM_004901.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr20:25203486 C>T maps to NM_001247.2 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr3:27758784 C>A maps to ENST00000449599 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2280-01A-01W-0799-08 chr3:27758584 A>C maps to ENST00000449599 Y698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1471-01A-01W-0551-08 chr22:41564511 C>T maps to NM_001429.3 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr12:132497561 C>T maps to ENST00000333577 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr20:34782203 G>A maps to NM_012156.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr20:34797483 C>T maps to NM_012156.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2540-01A-01D-1526-09 chr18:5489038 G>A maps to NM_012307.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr9:112042144 C>G maps to NM_019114.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr15:43500971 C>A maps to NM_000119.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr15:43498729 G>C maps to NM_000119.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr15:43507497 G>T maps to NM_000119.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr10:32581523 G>T maps to NM_025209.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr7:37960417 A>C maps to NM_017549.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr7:143098563 G>A maps to NM_005232.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr1:38185712 C>T maps to NM_001099439.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr1:38197200 G>A maps to NM_001099439.1 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1109-01A-01W-0484-10 chr3:89448465 A>G did not map to a codon.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr3:89499496 G>A maps to NM_005233.5 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr3:89259416 T>G maps to NM_005233.5 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr3:89456452 C>T maps to NM_005233.5 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr4:66217169 T>C maps to NM_004439.5 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr4:66242741 G>A maps to NM_004439.5 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr3:96706220 A>G maps to NM_001080448.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr3:97439133 C>A maps to NM_001080448.2 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr6:93979276 A>T maps to NM_004440.3 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr1:22915415 G>A maps to NM_020526.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr3:134920467 C>T maps to NM_004441.4 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr1:23208912 G>A maps to ENST00000400191 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr7:100411572 C>G maps to NM_004444.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr1:226019477 A>T did not map to a codon.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr17:48618163 G>A maps to NM_017957.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr1:220162111 T>C maps to NM_004446.2 K865K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr19:16552986 A>G did not map to a codon.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr19:16528757 C>A did not map to a codon.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr19:16552783 C>T maps to ENST00000455140 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1365-01A-01W-0490-10 chr1:110299772 G>T maps to NM_139053.1 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr1:110293398 A>C maps to NM_139053.1 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr13:43462621 A>G maps to NM_001002264.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr13:43566223 G>A maps to NM_001002264.1 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr13:43469189 G>A maps to NM_001002264.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr17:56280665 C>T maps to NM_000502.4 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr5:65317214 T>A did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr12:1553750 T>G maps to NM_178040.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr12:1346061 C>T maps to NM_178040.2 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr3:56330281 A>T maps to ENST00000460849 L280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1428-01A-01W-0549-09 chr3:56026089 C>G maps to ENST00000460849 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr3:56041291 T>G maps to ENST00000460849 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr2:128046407 G>A maps to NM_000122.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr16:14041792 C>T maps to NM_005236.2 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr16:14029159 C>T maps to NM_005236.2 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr13:103528186 C>T maps to NM_000123.2 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr10:50708698 G>A maps to NM_000124.2 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr10:50701241 C>T maps to NM_000124.2 W581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr10:50738886 C>A did not map to a codon.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr23:71424879 T>G did not map to a codon.
Sequencing variant TCGA-23-1026-01B-01W-0484-10 chr23:71426274 G>A did not map to a codon.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:71425401 C>G did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr23:71427732 G>C did not map to a codon.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr5:172324047 G>A maps to NM_001031711.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr12:29510634 T>G maps to NM_016570.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr1:44778839 C>G did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr2:54028848 G>A did not map to a codon.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr2:54035461 G>A maps to NM_015701.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr9:5801199 C>G maps to NM_024896.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr16:23706579 C>A maps to NM_033266.3 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr16:23716379 G>A maps to NM_033266.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr14:53119982 G>A maps to NM_014584.1 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr1:236389792 C>T maps to NM_019891.3 W276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr6:11104775 G>C maps to NM_207582.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr13:47361168 C>A maps to NM_001984.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr12:53676142 G>A maps to NM_012291.4 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr16:68265860 C>G maps to NM_024939.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr23:103495038 G>A did not map to a codon.
Sequencing variant TCGA-24-1471-01A-01W-0551-08 chr12:56532264 G>A maps to NM_001184796.1 E815E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr12:56531356 G>A maps to NM_001184796.1 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr5:137854396 G>T maps to NM_004730.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr1:157067660 G>A maps to NM_001004341.2 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr17:41606538 C>G maps to NM_001079675.1 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr3:185823280 T>A maps to NM_004454.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr4:5733348 G>T maps to NM_153717.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0891-01A-01W-0420-08 chr19:7912659 C>T maps to NM_001159944.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr17:74017578 G>C maps to NM_001988.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:176945476 G>T maps to NM_001080458.1 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr2:176947136 C>A maps to NM_001080458.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr14:57710914 A>G maps to ENST00000340918 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr1:231471868 G>A maps to NM_175876.3 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:11129694 C>T maps to NM_001001998.1 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr8:145135278 G>A maps to NM_019037.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr8:118825128 C>T maps to NM_000127.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr8:119122832 C>T maps to NM_000127.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr20:45725728 G>C maps to ENST00000360649 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr6:66112465 T>G maps to ENST00000370616 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr6:159206612 C>A maps to NM_001111077.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr5:76028928 C>T maps to NM_001992.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr1:169521972 C>G did not map to a codon.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr23:154156921 G>A did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:154090036 C>G did not map to a codon.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:154158084 G>A did not map to a codon.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr23:154133085 C>A did not map to a codon.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr23:154185253 G>T did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr23:154227759 A>T did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr23:154134846 C>T did not map to a codon.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr23:138623283 G>C did not map to a codon.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:57358059 C>T did not map to a codon.
Sequencing variant TCGA-24-0975-01B-02W-0486-08 chr23:57473467 C>G did not map to a codon.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr23:57319014 T>G did not map to a codon.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr1:50941336 G>C maps to NM_007051.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr2:96076300 C>T maps to NM_016044.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr12:50282967 G>A maps to NM_012306.2 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr9:130716121 G>A maps to NM_001035254.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr9:130710665 C>A maps to NM_001035254.2 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr1:109171421 G>A maps to NM_001010883.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr5:14681610 G>T maps to NM_138348.4 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr19:1877544 G>A maps to NM_031213.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr11:58893254 G>A maps to NM_198947.3 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr20:2819115 G>A maps to NM_022760.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr12:47629949 C>T maps to NM_138371.1 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr12:47629391 G>T maps to NM_138371.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr5:153372544 T>C maps to ENST00000442256 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr7:143573338 G>T maps to NM_014719.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr2:203630304 A>T maps to NM_173511.3 K530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr2:208488952 C>T maps to ENST00000272839 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr23:54106712 T>A did not map to a codon.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr23:54143029 G>A did not map to a codon.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr23:54161318 C>G did not map to a codon.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr23:54161409 G>T did not map to a codon.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr23:54209005 G>A did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr23:54099580 G>C did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr13:25743798 G>T maps to NM_152704.2 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr23:63410535 G>A did not map to a codon.
Sequencing variant TCGA-13-0889-01A-01W-0419-10 chr23:63412537 G>A did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:63410073 G>C did not map to a codon.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr23:63412869 C>A did not map to a codon.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr2:225266121 G>A maps to NM_001122779.1 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr7:23017920 G>T maps to NM_032581.3 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr7:22985375 C>T maps to NM_032581.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr23:134156167 C>G did not map to a codon.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr5:16572165 G>A maps to NM_001034850.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr8:139180267 G>A maps to NM_015912.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr8:139180201 G>A maps to NM_015912.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr8:139163522 G>A maps to NM_015912.3 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr8:139165262 A>G maps to NM_015912.3 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr8:139153453 G>C maps to NM_015912.3 T1259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr8:139144850 G>T maps to NM_015912.3 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr8:139164353 G>T maps to NM_015912.3 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr4:89709063 G>A maps to NM_014883.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr4:187086539 G>A maps to ENST00000356371 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr5:175520249 A>T maps to NM_001079529.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr13:108518299 G>C maps to NM_001080396.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr23:68749520 A>G did not map to a codon.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr23:68748886 G>A did not map to a codon.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr2:62067259 G>C maps to ENST00000404929 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:62067424 T>A maps to ENST00000404929 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr3:122123189 T>C maps to NM_014367.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr10:15296824 C>A maps to NM_001010924.1 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr2:187627364 G>T maps to NM_177454.3 G766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr2:187605045 G>A maps to NM_177454.3 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0968-01A-01W-0484-10 chr2:29249829 G>A maps to NM_199280.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr1:43616453 C>G maps to NM_001101376.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr1:43621953 G>A maps to NM_001101376.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr19:35715949 G>A maps to NM_152481.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr10:15876567 C>T maps to NM_024948.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr1:155218026 C>G maps to ENST00000368370 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr4:2698259 C>T maps to ENST00000324666 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr4:2696852 C>A maps to ENST00000324666 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr3:150377800 T>A maps to NM_152394.3 K624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr10:128974314 G>T maps to NM_001039762.2 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr23:103434384 T>C did not map to a codon.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr3:68466562 C>T maps to NM_213609.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr10:51892656 G>A maps to NM_001005751.1 K1326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr10:47911506 G>A maps to NM_018232.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr10:47935537 A>G maps to NM_018232.1 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr9:97081160 A>T maps to NM_017561.1 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr10:124672469 A>T maps to NM_001029888.1 *106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr18:10691283 G>A maps to NM_022068.2 R2317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr1:110587642 G>A maps to NM_033088.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:34148303 A>T did not map to a codon.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr23:34150180 C>T did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:34148342 A>G did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr23:34148799 C>T did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr23:34148346 C>T did not map to a codon.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr23:34148897 G>A did not map to a codon.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr23:34148258 G>T did not map to a codon.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr23:34149720 C>T did not map to a codon.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr23:34962095 G>A did not map to a codon.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr23:34962305 C>G did not map to a codon.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr23:34962067 C>A did not map to a codon.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr23:34961819 G>A did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr23:34962024 C>T did not map to a codon.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:37028940 G>A did not map to a codon.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr23:37028412 C>G did not map to a codon.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:37027636 C>A did not map to a codon.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr23:37028283 A>G did not map to a codon.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr23:37027376 T>C did not map to a codon.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr23:37026704 C>T did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:37027235 C>A did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr2:16743397 G>A maps to NM_030797.3 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr23:153674897 G>A did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr5:137682560 G>T maps to NM_001135647.1 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr5:137681225 T>G maps to NM_001135647.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr16:67576752 C>T maps to NM_001193523.1 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr16:67576922 C>A maps to NM_001193523.1 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1950-01A-01W-0699-08 chr20:49236587 C>T maps to NM_080829.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr1:212798350 G>A maps to NM_153606.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr5:156590504 A>T maps to NM_130899.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr5:156590101 C>A maps to NM_130899.2 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr5:156589769 G>A maps to NM_130899.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr14:67671409 C>T maps to NM_173526.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr15:59752329 C>T maps to NM_152450.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr2:38179074 C>A maps to NM_144713.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr8:87498712 C>T maps to NM_016033.2 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr6:54804998 T>C maps to NM_001010872.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr6:54806237 A>G maps to NM_001010872.1 K823K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr6:54806537 T>G maps to NM_001010872.1 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr6:54735463 G>A maps to NM_001010872.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr20:33874442 C>G maps to NM_178468.4 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr20:33874559 G>T maps to NM_178468.4 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr20:37580953 G>T maps to NM_030919.2 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr19:49116422 C>T maps to NM_017708.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr17:18874743 C>T maps to NM_001039999.2 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr12:8377407 G>C maps to NM_018088.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr19:38899446 C>G maps to NM_174905.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr3:10106039 G>T maps to NM_033084.3 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr9:35076000 G>A maps to NM_004629.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr14:45645044 C>T maps to NM_020937.2 R1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr10:127697034 G>A maps to ENST00000368692 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr2:163059655 C>G did not map to a codon.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr2:163099433 G>A maps to NM_004460.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr13:99092291 C>T maps to NM_005766.2 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr2:242402803 C>T maps to NM_014808.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr19:13033678 G>C maps to NM_004461.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr19:13034962 A>T did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr19:13035071 C>T maps to NM_004461.2 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr17:80041396 C>T maps to NM_004104.4 P1779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr2:170393764 C>T maps to NM_024622.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr2:207636733 G>C maps to NM_014929.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr5:7867143 A>G maps to NM_024091.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr5:7867092 A>G maps to NM_024091.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr5:7866094 A>T maps to NM_024091.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr5:7867011 A>C maps to NM_024091.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr4:187510153 G>T maps to ENST00000260147 P4456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr4:187540677 C>T maps to ENST00000260147 R2357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr4:187630465 G>A maps to ENST00000260147 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr4:187629979 G>C maps to ENST00000260147 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr5:150934012 G>A maps to NM_001447.2 D1285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr5:150920313 G>T maps to NM_001447.2 P2951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr5:150901461 C>G maps to NM_001447.2 L3564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr5:150891888 A>G maps to NM_001447.2 D3914D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr5:150924641 G>A maps to NM_001447.2 Q2016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr11:92568102 C>A maps to ENST00000298047 A3313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr11:92533846 A>G maps to ENST00000298047 E2556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr11:92495128 C>A maps to ENST00000298047 Y1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr11:92533258 C>T maps to ENST00000298047 C2360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr4:126241924 T>A maps to NM_024582.4 G1453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr4:126240976 T>C maps to NM_024582.4 Y1137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr4:126372409 C>A maps to NM_024582.4 I3413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr4:126372376 C>T maps to NM_024582.4 P3402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr4:126240547 A>G maps to NM_024582.4 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr4:126241591 C>T maps to NM_024582.4 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1416-01A-01W-0549-09 chr23:150890392 A>C did not map to a codon.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr17:73922958 C>G did not map to a codon.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr14:92403370 G>C maps to ENST00000267620 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr15:48713001 G>A maps to NM_000138.4 D2567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr5:127685144 C>T maps to NM_001999.3 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr5:127710426 C>T maps to NM_001999.3 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr5:127712496 G>A maps to NM_001999.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr19:8155127 C>G maps to NM_032447.3 R2013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr19:8201404 G>A maps to NM_032447.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr19:8191367 G>A maps to NM_032447.3 C846C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr7:102518011 G>A maps to NM_145032.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr12:1702230 C>T maps to NM_152441.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr7:5540702 C>T maps to ENST00000312577 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr17:37425078 C>T did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr5:135273112 G>A did not map to a codon.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr6:99322165 G>A maps to NM_012160.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr4:15627590 C>T maps to NM_012161.3 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr18:71740791 C>A maps to NM_001142958.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr10:5948331 C>T maps to NM_032807.3 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr7:100190452 C>T maps to NM_012172.4 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr1:224318211 G>A maps to NM_015176.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr6:146127274 G>A maps to NM_032145.4 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr14:39900991 C>A maps to NM_203301.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr2:230875524 C>A maps to NM_174899.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr3:121341494 G>T maps to NM_016298.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr3:121341364 T>C maps to NM_016298.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr19:46215217 C>T maps to NM_001080469.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr4:153244204 A>T maps to NM_033632.2 L651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr4:153273825 A>C maps to NM_018315.4 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr12:117461993 G>T maps to NM_153348.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr19:12800619 C>G maps to ENST00000380339 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr19:55401078 C>T maps to NM_002000.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr19:40433674 G>A maps to NM_003890.2 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr1:161480678 G>A maps to NM_001136219.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr1:161514545 C>T maps to NM_000569.6 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr11:72554253 C>T maps to ENST00000409314 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:157771885 A>G maps to NM_052938.4 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr1:157773773 G>A maps to NM_052938.4 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr1:157648556 T>C maps to NM_052939.3 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr1:157512667 A>C maps to NM_031281.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2280-01A-01W-0799-08 chr1:157508936 G>A maps to NM_031281.2 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr5:114860859 A>T maps to NM_020177.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr2:97363279 C>T maps to NM_001113382.1 Y1394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr8:125047660 C>T maps to NM_001039112.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr8:125109588 G>A maps to NM_001039112.2 R1591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr7:19184739 G>A maps to NM_152898.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr11:125359622 G>C maps to NM_005103.4 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr2:36805937 G>T maps to NM_001042548.1 Y235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr7:121943233 C>T maps to NM_001024613.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr19:35849887 C>T maps to NM_005304.3 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr4:155508771 C>A maps to NM_000508.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr4:155505608 G>T maps to NM_000508.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:54473871 C>A did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:54472705 G>C did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:54482210 C>T did not map to a codon.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr23:54472830 C>T did not map to a codon.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr6:36979621 G>C maps to NM_173558.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr9:95765241 G>A maps to NM_033086.2 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr12:32751499 C>T maps to NM_139241.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr5:44305162 C>T maps to NM_004465.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr5:44305237 A>G maps to NM_004465.1 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr3:192078253 A>T maps to NM_021032.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr23:137715073 C>T did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr13:102379045 A>G maps to NM_175929.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr13:102527629 A>T maps to NM_175929.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr13:102375267 C>T maps to NM_175929.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr19:49259693 G>A maps to NM_019113.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr11:69625282 G>A maps to NM_005247.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr13:22275395 C>A maps to NM_002010.2 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr8:38275795 G>A maps to NM_001174067.1 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr10:123276863 G>C maps to ENST00000357555 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr5:176517631 G>A maps to NM_213647.1 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:60073476 C>T maps to NM_001113411.1 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr2:105990123 G>A maps to ENST00000344213 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr6:97051518 C>A maps to NM_020482.4 Y10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr16:67271276 C>A maps to NM_013241.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr23:15376213 G>A did not map to a codon.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr17:39976623 T>G maps to NM_021939.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr9:115950084 G>C maps to ENST00000446284 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr6:35604929 G>C maps to NM_001145775.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr19:18650468 G>C maps to NM_012181.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr1:152279336 A>G maps to NM_002016.1 A2675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr1:152286914 C>T maps to NM_002016.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr1:152286386 C>T maps to NM_002016.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr1:152279018 G>A maps to NM_002016.1 D2781D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr1:152275616 A>G maps to NM_002016.1 S3915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr1:152275826 G>A maps to NM_002016.1 S3845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr1:152285795 T>G maps to NM_002016.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr1:152323538 T>C maps to NM_001014342.2 T2241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr1:152324054 G>A maps to NM_001014342.2 H2069H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr11:128680372 G>A maps to NM_002017.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr11:128680519 C>T maps to NM_002017.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr14:21542963 G>T maps to NM_018071.3 G359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr9:84609602 G>A maps to NM_001001670.2 R1406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr9:84605811 C>T maps to NM_001001670.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr3:58109124 G>A maps to NM_001164317.1 E1144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr3:58116573 C>T maps to NM_001164317.1 F1443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr7:128478048 G>C maps to NM_001458.4 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr7:128477556 C>T maps to NM_001458.4 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1517-01A-01W-0615-10 chr14:86089195 C>T maps to NM_013231.4 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr14:86089684 C>T maps to NM_013231.4 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr14:86089003 G>A maps to NM_013231.4 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr20:14307300 A>G maps to NM_198391.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr13:28589291 A>C did not map to a codon.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr14:76107535 C>A maps to NM_017791.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr15:33066555 C>G did not map to a codon.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr1:240286638 G>A maps to ENST00000406993 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr1:240371921 C>A maps to ENST00000406993 G1413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr1:240370874 T>C maps to ENST00000406993 P1064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr2:153417432 C>T maps to NM_052905.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr2:153485023 G>T maps to NM_052905.3 E793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr1:171303864 A>G maps to NM_002022.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr23:147030281 G>A did not map to a codon.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr23:147009911 G>T did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:147024699 G>A did not map to a codon.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:147063125 C>A did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr23:147090190 G>C did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr2:216259410 A>G maps to NM_212482.1 P1212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr6:159670086 G>A maps to NM_032532.2 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr6:159636109 C>T maps to NM_032532.2 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr1:109271308 T>C maps to NM_001144937.1 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2000-01A-01W-0722-08 chr1:109273509 C>A maps to NM_001144937.1 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr17:33457377 C>T maps to NM_017559.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr11:89413789 G>A maps to NM_153696.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr11:89409337 T>A did not map to a codon.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr19:45973936 C>G maps to NM_006732.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr6:1611120 C>T maps to NM_001453.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr14:29237219 C>T maps to NM_005249.3 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr8:145701124 G>A maps to NM_003923.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr1:42671456 C>T maps to NM_001198850.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr17:80521409 C>A maps to NM_004514.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr12:2968343 A>G maps to NM_202002.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr12:2968073 T>C maps to NM_202002.1 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr12:2981333 T>G maps to NM_202002.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr12:2973659 C>G maps to NM_202002.1 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr13:41134758 G>T maps to NM_002015.3 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1672-01A-01W-0633-09 chr23:70321189 C>T did not map to a codon.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr23:70320729 C>T did not map to a codon.
Sequencing variant TCGA-23-1107-01A-01W-0484-10 chr3:71037143 C>T did not map to a codon.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr7:114302154 T>A maps to NM_148898.3 C586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr7:114174755 C>T maps to NM_148898.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr7:114284749 G>T maps to NM_148898.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr23:49113977 C>T did not map to a codon.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr23:49113428 C>T did not map to a codon.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr23:49110496 A>G did not map to a codon.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr6:41533623 G>C maps to NM_001012426.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr20:30432787 A>T maps to NM_004118.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr19:52250019 G>A maps to NM_002029.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr19:52272396 C>G maps to NM_001005738.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr4:79351518 G>A maps to NM_025074.6 Q1639Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr4:79399114 T>A maps to NM_025074.6 I2666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr13:39453023 C>A maps to NM_207361.4 A2972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr13:39338456 G>A maps to NM_207361.4 T1760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr4:190878563 T>A maps to NM_004477.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr9:85958174 C>T maps to NM_174938.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr3:69230515 C>T maps to NM_015123.1 K795K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr11:65172366 C>T maps to NM_031904.3 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr9:37744773 C>T maps to NM_014907.2 N915N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr23:12735838 C>A did not map to a codon.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr23:12734760 C>T did not map to a codon.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr23:12712556 A>G did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr23:12736741 C>A did not map to a codon.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr23:12708327 C>G did not map to a codon.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr13:32652986 C>T maps to NM_023037.2 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr13:32752459 C>G maps to NM_023037.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr13:32731425 C>T maps to NM_023037.2 Y556Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr7:5643563 C>T maps to ENST00000340250 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr7:127235906 G>T maps to NM_020369.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr11:30255217 T>C maps to NM_001018080.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr11:30253520 C>A maps to NM_001018080.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr2:49381478 A>T maps to NM_000145.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr15:39910271 C>A maps to NM_152597.4 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:48340872 G>T did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr17:61904238 G>C maps to NM_017647.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr6:37418055 T>C maps to NM_015050.2 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr16:70497547 G>T maps to NM_145059.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:154282919 A>G did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr8:33246747 A>C maps to ENST00000380081 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr3:180685968 A>T maps to NM_005087.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr17:7507344 C>T maps to NM_004860.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr5:39134989 C>A maps to ENST00000263405 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr17:42636600 G>A maps to NM_001466.3 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr17:42635859 A>G maps to NM_001466.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr23:153760228 G>A did not map to a codon.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr23:153760259 G>C did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:153760853 C>T did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:153762657 G>A did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:153760890 C>A did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:153944596 C>T did not map to a codon.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr6:29589567 T>A maps to NM_001470.2 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr6:29577124 G>C maps to NM_001470.2 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr6:29598264 G>A maps to NM_001470.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr6:29589552 A>G maps to NM_001470.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr5:161318057 T>A did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:151336920 C>T did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:151336983 C>T did not map to a codon.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr4:46979123 C>G maps to NM_000809.2 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr4:46976320 C>A maps to NM_000809.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr5:161128736 T>C maps to NM_000811.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr15:26793248 C>T maps to NM_021912.4 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr1:1961651 C>T maps to NM_000815.4 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1666-01A-01W-0615-10 chr23:151129760 A>G did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr23:151138158 A>T did not map to a codon.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr23:151131084 T>A did not map to a codon.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr23:151123993 C>T did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr23:151138671 G>A did not map to a codon.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr23:151124289 C>T did not map to a codon.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr4:46053581 C>T maps to NM_173536.3 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr5:161531030 C>A maps to NM_198903.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr5:161524810 C>A maps to NM_198903.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr23:151821310 A>G did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:151808925 A>G did not map to a codon.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr23:151815599 C>G did not map to a codon.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr3:97731369 G>A maps to NM_001105580.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr10:26575273 G>T maps to NM_001134366.1 G413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2436-01A-01D-1526-09 chr10:26508164 G>A maps to NM_001134366.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr19:13065201 G>C maps to NM_052850.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr7:99758525 C>T maps to NM_024637.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr7:99757777 C>A maps to NM_024637.4 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr15:49611853 C>T maps to NM_002044.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr18:33243590 G>C did not map to a codon.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr2:155099397 G>A maps to NM_052917.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr2:31168706 G>A maps to NM_024572.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr1:230338901 C>T maps to NM_004481.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr14:69808445 C>T maps to NM_020692.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr3:16261469 C>A maps to NM_054110.4 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr7:151711778 A>G maps to NM_145292.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr4:173730668 C>A maps to NM_001034845.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr11:62407100 G>A maps to NM_198335.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr11:62397884 C>G maps to NM_198335.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr11:62398581 G>C maps to NM_198335.2 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr17:34072742 G>T maps to NM_139285.2 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr16:90109665 C>T maps to NM_001481.2 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr10:8100550 G>A maps to NM_001002295.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr1:155207161 T>C maps to NM_001005742.2 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0364-01A-02W-0370-10 chr3:81640302 G>C maps to ENST00000264326 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr3:81586151 G>A maps to ENST00000264326 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr3:81754733 G>A maps to ENST00000264326 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr10:104111613 G>C maps to NM_004193.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr1:89522550 G>A maps to NM_002053.2 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr1:89478948 G>A maps to NM_018284.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:89730536 T>C maps to NM_052942.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr1:89846077 A>T maps to NM_198460.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr1:89637594 T>A maps to NM_207398.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr2:27722271 C>T maps to NM_001486.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr2:27729422 C>G maps to NM_001486.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr6:53373416 T>C maps to NM_001498.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr6:10875049 A>T maps to NM_004752.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr6:10874449 C>T maps to NM_004752.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr6:10875139 A>G maps to NM_004752.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr12:120600701 C>T maps to NM_006836.1 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr12:120595679 G>A maps to NM_006836.1 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr12:120575509 T>G maps to NM_006836.1 R2168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1575-01A-01W-0615-10 chr6:10557282 A>G maps to NM_001491.2 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr6:10586455 G>A maps to NM_145655.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr15:59910577 T>C maps to NM_004751.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr9:74840651 T>C maps to ENST00000238018 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr1:118449148 A>G maps to NM_017686.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr1:118424459 G>A maps to NM_017686.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr16:19528412 A>T maps to NM_016641.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr10:48416468 G>C maps to NM_016204.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr10:48413727 C>T maps to NM_016204.1 V380V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-30-1857-01A-02W-0639-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr20:34022099 C>T maps to ENST00000374375 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr8:97172701 G>A maps to NM_001001557.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr23:69646528 C>T did not map to a codon.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:69647009 G>T did not map to a codon.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr23:69647001 A>C did not map to a codon.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr11:76940192 A>C did not map to a codon.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr17:650076 G>A maps to NM_015721.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr17:42991125 C>T maps to NM_002055.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr17:42988740 C>T maps to NM_002055.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr1:92948577 C>G maps to NM_005263.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr3:158376727 A>G maps to ENST00000264263 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr3:158371185 T>C maps to ENST00000264263 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr16:67719597 C>A maps to NM_030819.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr10:117971141 C>A did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr10:117885054 G>C maps to NM_005264.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr5:137593527 G>C maps to NM_001496.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr5:137600067 C>T maps to NM_001496.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr16:23481340 G>T maps to NM_015044.4 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr17:73235512 T>A maps to NM_138619.2 K575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr17:73239645 C>A maps to NM_138619.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr17:73236435 C>T maps to NM_138619.2 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr22:24622736 T>C did not map to a codon.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr20:33442335 G>A maps to NM_178026.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr20:33440277 G>T maps to NM_178026.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr22:22989328 A>T maps to ENST00000215938 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr17:61994866 C>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr7:31008681 C>T maps to NM_000823.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr11:59612901 G>A maps to NM_005142.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr7:100279858 C>T did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr2:233660905 C>A maps to ENST00000373566 Y560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr2:233655522 G>C maps to ENST00000373566 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr7:150417433 G>A maps to NM_130759.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr7:150269274 C>T maps to ENST00000430830 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:150439379 C>G maps to ENST00000447239 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr7:150174228 G>A maps to NM_175571.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr19:46181162 G>C did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr6:90605257 A>C maps to NM_032602.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr1:147380441 T>G maps to NM_005267.4 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr1:147380990 G>A maps to NM_005267.4 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr1:35227196 G>A maps to NM_153212.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr3:141917754 T>C maps to NM_001039547.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr11:134241660 A>C maps to NM_138342.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr11:134177016 G>T did not map to a codon.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr15:69560790 G>T maps to NM_015554.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr15:51687158 C>T maps to NM_181789.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr15:51676063 A>G maps to NM_181789.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr16:74499606 G>C maps to NM_012201.5 Y878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr16:74502930 G>A maps to NM_012201.5 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr12:57858597 G>A maps to NM_005269.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr2:121747794 C>T maps to NM_005270.4 D1435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr7:42006012 C>T maps to NM_000168.5 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr9:4117802 T>A maps to NM_001042413.1 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr1:92755767 C>T maps to NM_053274.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr17:9791265 G>A maps to NM_004246.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr23:14627258 G>A did not map to a codon.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr23:102979144 G>A did not map to a codon.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr12:129467529 C>T maps to ENST00000442111 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr19:17670131 C>T maps to NM_024656.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr9:138516110 T>C maps to NM_182974.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr10:88854397 C>A maps to NM_005271.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:120183097 A>C did not map to a codon.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr23:120182078 G>C did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr11:58711129 A>C maps to NM_080661.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr6:1930357 G>C maps to NM_001500.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr19:19745666 C>T maps to NM_016573.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr6:16290696 T>A maps to NM_006877.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr14:24706358 G>C did not map to a codon.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr3:155654194 C>T maps to NM_003875.2 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr3:155643133 A>G maps to NM_003875.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr9:80049380 C>A maps to NM_004297.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr1:110116389 G>A maps to NM_006496.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr18:11753898 C>T maps to NM_182978.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr20:57480493 C>G maps to NM_080425.2 Y806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr20:57480493 C>G maps to NM_080425.2 Y806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr20:57430053 A>G maps to NM_080425.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr20:57415358 C>T maps to NM_016592.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr1:1735945 G>A maps to NM_002074.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr7:93555455 G>A maps to NM_004126.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0891-01A-01W-0420-08 chr6:30521184 G>A maps to NM_005275.3 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr6:30521235 A>G maps to NM_005275.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr1:38040286 G>A maps to NM_013285.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:54584947 C>G did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr23:54586974 T>C did not map to a codon.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr1:231401854 G>T maps to NM_014236.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr4:44719162 T>A maps to NM_138335.1 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr12:102190521 G>A maps to NM_024312.4 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr12:102153833 G>A maps to NM_024312.4 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr16:1412860 G>T maps to NM_032520.4 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr4:68619927 A>G maps to NM_000406.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr15:74363967 C>T maps to NM_001038640.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr3:121410505 C>A maps to ENST00000393667 E2569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr5:32126329 C>T maps to NM_022130.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr1:155726841 C>T maps to ENST00000368331 L1808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr1:155726769 G>A maps to ENST00000368331 I1832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr2:171811158 G>C did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr17:45012462 C>T maps to NM_054022.2 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr16:20327316 G>A maps to NM_001007240.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr19:55525890 C>T maps to NM_001083899.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr1:156568826 G>A maps to NM_182679.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr1:46120313 G>A maps to NM_021639.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr2:241402903 G>C maps to NM_002081.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr23:132887740 C>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr13:92408649 G>A maps to NM_004466.4 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr13:92408575 C>G maps to NM_004466.4 Y394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr12:50500684 C>A maps to NM_005276.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr2:157352563 G>A maps to NM_000408.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr7:1132410 C>T maps to NM_001505.2 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr19:34856215 A>G maps to NM_000175.3 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr23:48976066 G>T did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr23:48979002 C>T did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr6:24462986 T>A maps to NM_001503.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr7:23309693 A>G maps to ENST00000435486 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr2:207041526 G>A maps to NM_005279.3 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr23:136113067 A>T did not map to a codon.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr23:136113807 G>A did not map to a codon.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr23:136113602 G>C did not map to a codon.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr9:132853177 T>C maps to NM_001136557.1 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr12:123186798 C>G maps to NM_177551.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr12:123187812 C>T maps to NM_177551.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr12:123201266 C>T maps to NM_006018.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr6:46988486 C>A maps to ENST00000283297 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr23:135427510 C>T did not map to a codon.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr23:135390975 A>C did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr23:135427477 C>G did not map to a codon.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr23:135429257 C>T did not map to a codon.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr23:135428707 G>A did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:135485438 T>G did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr23:135428630 T>G did not map to a codon.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr23:135431844 G>A did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:135482200 T>G did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr2:26534165 G>A maps to NM_001145168.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr2:26534453 G>A maps to NM_001145168.1 H714H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr2:26534723 G>A maps to NM_001145168.1 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr6:47682261 G>A maps to NM_153838.3 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:129518829 G>T did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:129518508 G>A did not map to a codon.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr23:129518823 G>A did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr8:37697733 C>G maps to NM_032777.9 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr8:37690581 C>T maps to NM_032777.9 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr14:105518038 C>T maps to NM_013345.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr12:131488815 C>A maps to NM_198827.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr12:131466489 G>A maps to NM_198827.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr17:72368474 C>T maps to ENST00000440684 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr17:72363840 G>A maps to NM_181790.1 W66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr23:9711618 C>A did not map to a codon.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr23:9711701 G>A did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr3:154146462 G>T maps to NM_001038705.1 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr3:154147152 C>T maps to NM_001038705.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr3:119892317 C>T did not map to a codon.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr10:25887605 T>C maps to NM_020752.2 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr10:25887863 C>T maps to NM_020752.2 N1103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr8:145583349 C>T maps to NM_024531.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr8:145583843 C>G maps to NM_024531.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr8:145584054 C>T maps to NM_024531.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr23:53106089 G>T did not map to a codon.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:78427171 G>A did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:78427490 A>C did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr7:107114561 G>A maps to NM_005295.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr1:200843142 C>T maps to NM_005298.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr3:71804075 C>T maps to NM_018971.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr6:167570884 G>A maps to NM_005299.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr19:51274381 G>A maps to NM_001506.1 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0975-01B-02W-0486-08 chr23:41555952 C>G did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:41555340 G>A did not map to a codon.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr23:41554986 C>T did not map to a codon.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr7:124386665 G>A maps to NM_005302.2 N585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr2:133402827 G>A maps to NM_001508.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr19:46094335 G>A maps to NM_005282.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr11:60620802 C>A maps to NM_004778.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:150349105 C>T did not map to a codon.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr23:150348553 G>T did not map to a codon.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr2:231775371 G>A maps to NM_005683.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr6:110300599 G>A maps to ENST00000414000 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr6:97247256 G>A maps to NM_030784.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr4:8582891 C>T maps to NM_080819.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr12:123214523 G>A maps to NM_032554.3 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr23:41586608 A>C did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr11:94113377 G>T maps to NM_016540.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr11:94134395 C>T maps to NM_016540.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr12:54756633 G>T maps to NM_020370.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr7:112723804 A>G maps to NM_018970.6 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr16:57718386 T>C maps to NM_170776.4 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr16:57712215 G>T maps to NM_170776.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr5:89949494 T>C maps to NM_032119.3 N1368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr5:89938501 C>T maps to NM_032119.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr5:90049488 C>A maps to NM_032119.3 T3740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr5:89925303 T>A maps to NM_032119.3 L596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr5:89925250 A>T maps to NM_032119.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr23:101910811 G>C did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr23:101971319 T>G did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr23:101969951 C>G did not map to a codon.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr12:13061824 C>T maps to NM_003979.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr6:117113363 T>G maps to NM_148963.2 R908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr6:117121827 A>T maps to NM_148963.2 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1634-01A-01W-0615-10 chr6:117130581 A>G maps to NM_148963.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr5:176026589 G>T maps to NM_052899.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr5:176026541 G>A maps to NM_052899.2 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr4:90169017 C>T maps to NM_198281.2 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr16:46931606 C>T maps to NM_133443.2 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr14:65406265 G>C maps to NM_002083.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr6:28474134 C>A maps to NM_182701.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr6:28472113 G>A maps to NM_182701.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr11:123477357 C>T maps to ENST00000456860 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr3:113623064 A>G maps to NM_017577.4 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr7:50742218 A>G maps to NM_005311.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr2:165404235 G>A maps to NM_004490.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr2:165365060 C>A did not map to a codon.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr2:165349665 G>A maps to NM_004490.2 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr17:73316547 G>A maps to NM_002086.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr2:11761032 C>T maps to NM_014668.3 I1349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr8:102582622 G>A did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr5:153078455 C>T maps to NM_001114183.1 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr5:153144083 G>A maps to NM_001114183.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr5:153190616 C>T maps to NM_001114183.1 N851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr5:153190757 G>A maps to NM_001114183.1 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr23:122532557 A>G did not map to a codon.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr23:122561909 G>A did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr23:122538714 G>T did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr23:122532604 C>T did not map to a codon.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr23:122598935 T>A did not map to a codon.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr11:105769125 G>A maps to NM_000829.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr10:87484286 T>C maps to NM_017551.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr10:87487707 G>A maps to NM_017551.2 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr10:87675941 C>T did not map to a codon.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr4:94137989 G>T maps to NM_001510.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr6:102074300 A>T maps to NM_021956.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr6:102266270 C>G maps to NM_021956.4 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr1:37271783 G>A maps to NM_000831.3 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr1:37346430 G>A maps to NM_000831.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr1:37291202 C>A did not map to a codon.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr1:37346391 G>A maps to NM_000831.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr11:120702669 C>T maps to NM_014619.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr11:120776147 C>T maps to NM_014619.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr16:9857784 G>A maps to NM_000833.3 R1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr16:9892134 A>G maps to NM_000833.3 D785D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr12:13768456 G>T maps to NM_000834.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr17:72846012 G>A maps to NM_000835.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr19:48917362 G>C did not map to a codon.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr19:48922494 C>T maps to NM_000836.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr9:104432514 A>G maps to NM_133445.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr9:104335628 G>T maps to NM_133445.2 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr12:66856836 G>T maps to ENST00000359742 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr12:66849240 T>A maps to ENST00000359742 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr23:48831565 C>T did not map to a codon.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr23:48853698 C>T did not map to a codon.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr23:48855893 G>T did not map to a codon.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr10:121201574 C>G maps to NM_005308.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr19:47423158 C>A maps to NM_004491.4 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr19:47424859 G>A maps to NM_004491.4 P976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr19:47424885 C>G maps to NM_004491.4 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr19:47423687 C>T maps to NM_004491.4 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr19:47423033 A>T maps to NM_004491.4 K368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0927-01A-02W-0419-10 chr6:146350691 T>C maps to NM_000838.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr6:146351123 G>A maps to NM_000838.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr7:86468752 T>C maps to NM_000840.2 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr7:86469004 A>G maps to NM_000840.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr5:178413883 G>A maps to NM_000843.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr3:7620822 A>C maps to NM_181874.2 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr7:126173770 A>T maps to NM_001127323.1 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr7:126746619 C>T maps to NM_001127323.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr23:16168459 A>G did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr23:16168742 T>A did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:16168718 A>G did not map to a codon.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr13:114009662 G>A maps to NM_024719.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr14:95236244 C>T maps to NM_173849.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr8:130760776 G>C maps to NM_031415.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr8:130788400 G>T maps to NM_031415.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr8:130760842 C>T maps to NM_031415.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr16:27974489 C>A maps to NM_001109763.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr16:27818806 C>T did not map to a codon.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr19:42734951 G>A maps to NM_019884.2 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr9:124073038 G>A maps to NM_000177.4 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr16:11990466 C>A maps to NM_002094.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:51488455 A>T did not map to a codon.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr23:51486769 C>T did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr1:110201707 G>A maps to NM_000850.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr11:67353897 G>T maps to NM_000852.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr22:24376833 C>T maps to NM_000853.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr13:28368001 A>T maps to NM_145657.1 K238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr2:48848421 G>A maps to NM_172311.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:48873703 A>G maps to NM_172311.2 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr1:89323152 G>A maps to NM_001514.5 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr1:89325690 G>A maps to NM_001514.5 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr6:30880174 G>T maps to NM_001517.4 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr7:74005217 C>T maps to NM_016328.2 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr7:74005217 C>T maps to NM_016328.2 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr7:74236961 A>G maps to NM_173537.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr16:27501065 T>A did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr16:27549655 G>A maps to NM_001520.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1995-01A-01W-0722-08 chr2:197664242 G>C maps to NM_012086.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr10:1046801 C>T maps to NM_012341.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1672-01A-01W-0633-09 chr20:60776027 G>A maps to NM_015666.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr20:60775754 C>T maps to NM_015666.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr11:106647284 G>A maps to ENST00000282249 Y572Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr11:106810881 T>C maps to ENST00000282249 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr12:14794028 A>G maps to NM_004963.3 C685C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr12:14827687 G>A maps to NM_004963.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr23:108636262 T>C did not map to a codon.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr23:108647660 C>T did not map to a codon.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr23:108673620 T>A did not map to a codon.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr3:148744620 G>C maps to NM_004130.3 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr23:2774570 A>T did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr11:45948275 G>A maps to NM_152312.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr4:145038081 G>C maps to NM_002099.6 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1116-01A-01W-0486-08 chr19:49489139 G>A maps to NM_002103.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr19:49472859 C>A maps to NM_002103.4 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr19:49496303 G>A maps to NM_002103.4 F22F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-24-1614-01A-01W-0552-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr23:103268204 G>T did not map to a codon.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr10:115338450 C>T maps to NM_004132.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr10:115343115 T>C maps to NM_004132.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr9:99227687 C>G maps to NM_014282.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr4:108955464 G>A maps to ENST00000351726 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr2:26496569 C>T maps to NM_000183.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr12:96370401 G>A maps to NM_002108.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr1:156593710 C>A maps to NM_021817.2 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr5:140054613 A>G maps to NM_002109.3 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr8:122641137 C>T maps to NM_005328.2 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr4:2242553 C>A maps to NM_024511.5 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr14:23417106 C>A maps to NM_017815.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr6:135287502 G>A maps to NM_006620.3 Y669Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr1:110950281 G>C maps to NM_006402.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr23:153236182 G>A did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr23:153222893 T>C did not map to a codon.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr23:153222425 T>A did not map to a codon.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr23:153222915 G>A did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr12:104473357 T>C maps to NM_013320.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr5:45262304 C>T maps to NM_021072.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr1:155254397 C>T maps to NM_020897.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr15:73617476 C>T maps to NM_005477.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr15:73621967 G>A maps to NM_005477.2 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr6:55113536 T>G maps to NM_001526.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr6:55120145 C>A maps to NM_001526.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr6:55119998 C>T maps to NM_001526.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr3:13538270 C>T maps to NM_024827.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr5:141009425 C>A did not map to a codon.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr2:240024583 G>A maps to NM_006037.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr17:42188139 C>T maps to NM_001015053.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr23:48664775 C>T did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr23:48674575 T>C did not map to a codon.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr23:48678566 C>A did not map to a codon.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr23:48678596 G>A did not map to a codon.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr23:48682135 G>A did not map to a codon.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr23:83724006 T>C did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:83723898 G>A did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr1:236718740 T>C maps to NM_018072.5 E1926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr1:236757340 C>A maps to NM_018072.5 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr14:31778257 T>C maps to ENST00000389961 E1518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr2:37255208 G>T maps to NM_019024.1 S1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr2:37215846 C>T maps to NM_019024.1 A1951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr5:41061677 G>T maps to ENST00000296803 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr5:41033154 A>T maps to ENST00000296803 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr14:31604772 G>A maps to NM_015382.2 R1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr7:43590041 A>T did not map to a codon.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr7:43484246 G>A maps to NM_015052.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr7:43546772 C>A maps to NM_015052.3 Y1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr7:43581521 G>A maps to NM_015052.3 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr2:197184551 G>A maps to NM_020760.1 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr2:197171941 G>A maps to NM_020760.1 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr2:197085578 C>T maps to NM_020760.1 K1411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr3:124732832 G>T maps to NM_020733.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr3:124748075 C>T maps to NM_020733.1 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr10:96341235 T>C maps to NM_018063.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr4:84337943 G>C maps to NM_133636.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr7:92825176 T>C maps to ENST00000453812 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr7:92844714 A>T maps to ENST00000453812 Y261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr23:65412029 G>A did not map to a codon.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr23:65417689 C>T did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:65417597 C>T did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:65409633 C>T did not map to a codon.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr23:65390481 G>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:65392394 C>G did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr11:124789843 C>T maps to NM_001037558.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr15:63952071 A>C maps to ENST00000261887 L3096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr15:63964732 T>G maps to ENST00000261887 A2669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr15:63958317 G>A maps to ENST00000261887 I2785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr15:64005760 A>G maps to ENST00000261887 P1418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1771-01A-01W-0633-09 chr15:63964714 C>A maps to ENST00000261887 V2675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr15:28414685 C>A maps to NM_004667.4 L3391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr15:28459290 G>A maps to NM_004667.4 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr15:28474389 C>T maps to NM_004667.4 Q1741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr15:28508280 C>G maps to NM_004667.4 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr4:89625684 G>A maps to NM_014606.1 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr4:89407375 T>C maps to NM_016323.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr7:35709887 G>C maps to NM_022373.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr7:35674034 G>A maps to NM_022373.4 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr3:193854817 G>A maps to NM_005524.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr15:72638892 G>A maps to ENST00000457859 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr1:40105267 G>A maps to NM_014571.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr1:91809026 G>A maps to NM_001017975.3 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr1:91781478 T>C maps to NM_001017975.3 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr1:91731664 C>T did not map to a codon.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr7:81336663 C>A maps to NM_000601.4 G520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr7:81358973 C>T maps to NM_000601.4 W329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr17:79653371 G>A maps to NM_004712.4 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr3:42739825 G>A maps to NM_020707.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr4:145633224 T>C did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr9:97200741 G>A maps to NM_032558.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr9:97207274 C>T maps to NM_032558.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr7:27689214 T>C maps to NM_152740.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr7:75192533 C>T maps to NM_005338.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr12:123340854 T>C maps to NM_003959.1 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr12:123332625 G>T maps to NM_003959.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr1:114483214 C>G maps to ENST00000426820 Y141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr7:139299209 G>C maps to NM_022740.4 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr11:33374957 C>T maps to NM_005734.3 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr19:40895776 G>A maps to NM_144685.3 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr22:19396099 C>T maps to NM_003325.3 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr6:26056014 C>G maps to NM_005319.3 *214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr6:26056314 C>A maps to NM_005319.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr6:26056536 C>T maps to NM_005319.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr6:26199360 C>T maps to NM_021065.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr6:27860666 G>T maps to NM_003514.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr6:26123775 G>A maps to NM_003526.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr6:26158750 C>G maps to NM_138720.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr6:26184079 G>T maps to NM_003523.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr6:26252060 G>C maps to NM_003524.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr6:27100451 G>A maps to NM_021058.3 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr6:27100196 G>C maps to NM_021058.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr6:27861368 C>G maps to NM_003527.4 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr6:26197304 C>G maps to NM_003530.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr6:27778120 G>T maps to NM_003536.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr6:27858543 G>C maps to NM_003535.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1558-01A-01W-0615-10 chr6:26205069 G>C maps to NM_003545.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr1:149859163 G>T maps to NM_175065.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr1:149858596 C>T maps to NM_003517.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr1:228645227 C>T maps to NM_033445.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr6:12120831 T>C maps to NM_002114.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr6:12163571 A>C maps to NM_002114.2 A2345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr6:12124077 C>T maps to NM_002114.2 G1350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2355-01A-01W-0799-08 chr1:42049462 C>A maps to NM_024503.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr10:71026380 G>A maps to NM_025130.3 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr6:33036865 G>C maps to NM_033554.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr6:33043848 C>A maps to NM_002121.4 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr6:30460342 G>A maps to NM_005516.5 E354E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr17:53398035 C>T maps to NM_002126.4 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr1:221053252 G>T maps to NM_021958.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:186151414 C>T maps to NM_031935.2 C5470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr1:185834949 A>C maps to NM_031935.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr1:186113320 C>T maps to NM_031935.2 S4647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr1:186039780 A>G maps to NM_031935.2 P2677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr1:186043907 G>A maps to NM_031935.2 A2725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr1:185987406 C>G maps to NM_031935.2 S1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr1:186092233 C>T maps to NM_031935.2 V4127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0889-01A-01W-0419-10 chr1:186113407 G>A maps to NM_031935.2 A4676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr1:185992265 C>T maps to NM_031935.2 H1910H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr1:186056440 A>T maps to NM_031935.2 K3047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr1:186059938 T>C maps to NM_031935.2 L3259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr1:186084056 C>T maps to NM_031935.2 R3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr1:186135337 G>C maps to NM_031935.2 G5114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr15:77763380 C>T maps to NM_018200.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr13:31037342 C>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:150154643 A>T did not map to a codon.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:150156338 A>G did not map to a codon.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr23:150155687 G>T did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr6:55378916 G>T maps to NM_019036.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:120295936 G>A maps to NM_005518.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr1:120306816 C>T maps to NM_005518.3 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr5:162910279 T>A maps to NM_001142556.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr22:35782808 C>T maps to NM_002133.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr12:121434119 C>T maps to NM_000545.5 S337S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-04-1338-01A-01W-0484-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr20:43057023 G>A maps to ENST00000338692 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr5:137089047 G>A maps to NM_006805.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr13:53217389 G>T maps to NM_001011725.1 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr7:26233225 G>C maps to NM_031243.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr2:178082445 C>T maps to NM_194247.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr4:83278045 A>G maps to NM_031370.2 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr23:100667420 G>T did not map to a codon.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr10:70101809 G>C maps to NM_012207.2 *347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr19:39338014 C>A maps to ENST00000221419 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr19:39327370 G>A maps to ENST00000221419 H587H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr19:12881806 G>A maps to NM_013312.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr19:12875678 G>A maps to NM_013312.2 D592D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr8:42814396 A>C maps to NM_032410.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr1:150680807 A>T maps to NM_032132.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr7:27134976 G>T maps to NM_005522.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr7:27141070 G>A maps to NM_006735.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr7:27187350 C>T maps to NM_024014.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr1:33354678 C>T maps to NM_002143.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr10:100189399 C>T did not map to a codon.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr3:148885738 G>A maps to NM_032383.3 E952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0717-01A-01W-0370-10 chr3:148868391 C>T maps to NM_032383.3 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr22:26860098 T>C maps to NM_022081.4 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr10:103826235 G>C maps to NM_024747.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr11:6461905 C>G maps to NM_000613.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr8:21981312 G>A maps to NM_005144.4 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr5:175110475 G>C maps to NM_001131055.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr1:152193690 A>G maps to NM_001009931.1 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:152191032 A>T maps to NM_001009931.1 Y1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:152193030 G>A maps to NM_001009931.1 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr8:99116772 C>G did not map to a codon.
Sequencing variant TCGA-36-1575-01A-01W-0615-10 chr2:20818990 A>T maps to NM_022460.3 L312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:87558327 G>A maps to NM_012262.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr16:22926411 C>T maps to NM_006043.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:26147164 C>T maps to NM_006040.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr6:114378543 C>T maps to NM_153612.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr16:1961683 C>T maps to ENST00000454677 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr9:99003177 T>C maps to NM_000197.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr1:162773312 G>A maps to NM_016371.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr1:120050201 T>C maps to ENST00000235547 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr1:119964948 T>C maps to NM_000198.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr21:45050275 C>T maps to NM_007031.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr17:56557476 G>A maps to NM_001080439.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr10:118434747 G>A maps to NM_025015.2 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr6:31785269 G>A maps to NM_005345.5 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr6:31778435 G>T maps to NM_005527.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr4:128715244 T>C maps to ENST00000438626 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr9:127998912 G>A maps to NM_005347.4 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr11:111784460 C>A maps to NM_001541.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr17:40275326 G>A maps to NM_033194.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr3:122487637 T>A maps to NM_024610.4 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr1:22213973 G>C maps to NM_005529.5 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr1:22205080 G>T maps to NM_005529.5 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr1:22157544 G>A maps to NM_005529.5 Y3867Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:135579850 G>C did not map to a codon.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:135593244 C>A did not map to a codon.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr23:135592336 C>T did not map to a codon.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr23:135579861 G>C did not map to a codon.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr23:135593896 G>C did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr6:87725690 C>T maps to NM_000865.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1350-01A-01W-0490-10 chr13:47466627 C>T maps to NM_000621.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:113965829 T>A did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr23:114141163 C>T did not map to a codon.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr23:114141778 C>T did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:113965730 C>A did not map to a codon.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr23:114141222 G>A did not map to a codon.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr23:114141606 C>G did not map to a codon.
Multiple mappings detected for codon TCGA-30-1857-01A-02W-0639-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-61-1910-01A-01W-0639-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr1:20005163 G>A maps to NM_000871.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr10:92509272 G>A maps to NM_019859.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr4:8305997 T>G maps to NM_053044.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr4:3129255 G>A maps to NM_002111.6 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr4:3188379 G>A maps to NM_002111.6 L1641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr7:48018115 C>T maps to NM_004507.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:53607798 G>C did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr23:53571651 A>T did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:53577910 C>G did not map to a codon.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr23:53612054 A>T did not map to a codon.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr23:53578150 C>A did not map to a codon.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr23:53602135 A>G did not map to a codon.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr23:53655544 G>T did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:53622189 A>G did not map to a codon.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr23:53576263 G>T did not map to a codon.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr23:53577920 T>C did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:53578126 C>A did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:53672375 C>A did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr23:53563448 T>A did not map to a codon.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr23:53579650 C>T did not map to a codon.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr3:50357665 C>G maps to NM_033158.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr3:50332883 C>G maps to NM_003549.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr16:71163563 G>A maps to NM_032821.2 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr16:71026022 T>C maps to NM_032821.2 A1245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr16:71065634 A>G maps to NM_032821.2 T905T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr16:71059321 C>T maps to NM_032821.2 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr16:71096070 C>T did not map to a codon.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr16:70937537 A>G maps to NM_032821.2 L2946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr6:82924179 G>A maps to NM_015525.2 N656N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr17:62082580 G>A maps to NM_001099789.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr19:10398776 G>A maps to NM_001544.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr6:19838209 G>A maps to NM_001546.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr15:78452526 A>T maps to NM_005530.2 K90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr15:78452453 G>A maps to NM_005530.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr23:148568524 G>C did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr6:30712168 C>A maps to NM_003897.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr1:159023471 G>A maps to ENST00000295809 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr9:21227986 G>A maps to NM_021268.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr9:21187175 G>A maps to NM_021068.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr21:34725116 G>C maps to NM_000629.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr6:137519662 C>T maps to NM_000416.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr21:34787246 C>T maps to ENST00000381995 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr9:21141413 A>T maps to NM_002177.1 C52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr16:1636196 T>G maps to NM_014714.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr3:159997076 C>T maps to ENST00000483754 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr15:65624295 C>T maps to NM_004884.3 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr7:23383390 C>T maps to NM_006547.2 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr7:23381703 A>C maps to NM_006547.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr6:160517552 C>T maps to NM_000876.2 F2246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:130412649 G>T did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:130417180 T>C did not map to a codon.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr23:130408593 G>C did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr23:130408642 G>C did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr1:18703370 C>T maps to NM_032880.4 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr11:18739640 C>G did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr11:18730932 C>T did not map to a codon.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr16:21658718 G>A maps to NM_005849.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr11:133791090 G>A maps to NM_014987.1 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr11:133801002 G>A maps to NM_014987.1 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1494-01A-01W-0545-08 chr9:111651665 C>G maps to NM_003640.3 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr9:111640960 C>T maps to NM_003640.3 E1214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr1:206653228 C>T maps to NM_014002.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr1:206658351 A>G maps to NM_014002.3 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr1:206666628 C>T maps to NM_014002.3 Q655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr23:153770591 G>A did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:206945707 G>A maps to NM_000572.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr11:117869479 A>T maps to NM_001558.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr11:117870265 C>A maps to NM_001558.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr19:18183146 C>A maps to NM_005535.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr23:114245330 A>G did not map to a codon.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr15:81585209 G>A maps to NM_172217.3 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr22:17582933 G>A did not map to a codon.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr3:9949954 G>T maps to NM_153483.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr2:113675239 G>A maps to NM_014439.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr2:113783779 C>T maps to NM_014438.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr2:113742454 C>A maps to NM_019618.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr23:29935624 G>T did not map to a codon.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:29972756 G>A did not map to a codon.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr23:29972792 T>A did not map to a codon.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:29938192 G>A did not map to a codon.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr23:29938088 A>C did not map to a codon.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr23:29938202 A>C did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr23:29935616 G>C did not map to a codon.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr23:104440383 C>A did not map to a codon.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr23:104984675 G>A did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:105011402 C>T did not map to a codon.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr23:105011287 T>A did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr6:137322973 C>T maps to NM_014432.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr3:136708313 C>T maps to NM_144717.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr16:27456570 G>A maps to NM_181079.4 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1026-01B-01W-0484-10 chr1:67648525 A>T maps to NM_144701.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr14:23844832 G>A did not map to a codon.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr14:23844875 C>T maps to NM_022789.3 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr12:68619500 C>A maps to NM_018402.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr19:39760394 G>A maps to NM_172138.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr5:131398244 C>A maps to NM_000588.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr5:131398378 C>A maps to NM_000588.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:1497643 G>C did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr1:154437777 G>A maps to NM_000565.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr1:154420631 G>T maps to NM_000565.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr5:55259233 T>A maps to NM_002184.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr4:74607376 C>A maps to NM_000584.2 C61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr23:155240026 A>G did not map to a codon.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr1:166905933 G>A maps to NM_199351.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr19:10789295 A>G maps to NM_017620.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr19:10793340 C>T maps to NM_017620.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr19:10792756 G>A maps to NM_017620.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr2:239092347 C>T maps to NM_030768.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr19:15228698 A>T maps to NM_006844.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr7:128035055 C>T maps to NM_000883.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr3:49064164 A>G maps to NM_000884.2 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr6:76751727 G>A maps to NM_001563.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr6:76728497 C>T maps to NM_001563.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr1:62271126 C>G maps to NM_176877.2 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr1:62228764 T>C maps to NM_176877.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr15:41276059 G>A maps to NM_017553.1 D1379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr2:233990541 C>G maps to ENST00000359570 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr10:121586928 G>A maps to NM_014937.2 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr11:71939236 T>C maps to NM_001567.3 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr11:71945598 C>G maps to NM_001567.3 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:118864311 G>T did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr9:5185595 G>T maps to NM_007179.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr20:20350305 C>G maps to NM_002196.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr19:7163163 G>C maps to NM_000208.2 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr19:7143007 G>A maps to NM_000208.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr8:19675161 A>G maps to NM_018142.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr1:153724879 C>T maps to ENST00000428986 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr11:77672103 G>C maps to NM_033547.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr11:77639495 G>A maps to NM_033547.3 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr11:62416831 G>A maps to NM_030628.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr11:62414728 C>G maps to NM_030628.1 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr9:103004891 G>A maps to NM_014425.2 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr3:48726976 G>A maps to ENST00000395509 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr14:24652250 G>A maps to ENST00000458132 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1672-01A-01W-0633-09 chr11:9466731 G>A maps to NM_006391.2 G1036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr1:201842037 G>T maps to NM_018085.4 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr1:32672630 C>T maps to NM_001160042.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr12:113645404 C>T maps to ENST00000416617 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr15:67786631 C>T maps to NM_001031715.2 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr16:19741750 G>T did not map to a codon.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr5:75866443 C>T maps to NM_006633.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr1:156503592 C>T maps to NM_178229.4 G1316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr1:156521874 G>C maps to NM_178229.4 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr1:156533014 G>A maps to NM_178229.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr1:156503657 C>A maps to NM_178229.4 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr1:156496298 G>A maps to NM_178229.4 N1625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr1:156513970 C>T maps to NM_178229.4 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr23:53270967 C>A did not map to a codon.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr23:53283900 C>T did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr23:53280308 C>T did not map to a codon.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr23:53268468 T>C did not map to a codon.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr7:123101472 G>A maps to NM_178827.4 Q649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr23:153284905 G>A did not map to a codon.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr23:153278664 C>T did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:153284522 G>A did not map to a codon.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr3:10283842 G>A maps to NM_001570.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr4:185339691 T>A maps to NM_002199.3 K120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr1:234743404 C>T maps to NM_182972.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr6:405066 G>A maps to NM_002460.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr19:44099166 G>A maps to NM_001007561.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr2:227660564 T>G maps to NM_005544.2 R964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr2:227662614 G>A maps to NM_005544.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr23:107977215 C>T did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr23:107977212 C>T did not map to a codon.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr23:107979366 C>A did not map to a codon.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr23:107978425 G>A did not map to a codon.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr23:107977382 C>T did not map to a codon.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr23:107976662 G>A did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:107977048 G>T did not map to a codon.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr23:107976435 C>G did not map to a codon.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr5:3599808 C>T maps to NM_024337.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr5:62072855 G>A did not map to a codon.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr22:35481508 G>A maps to NM_001008494.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr5:52363080 C>T maps to NM_002203.3 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr17:42455064 C>T did not map to a codon.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr17:42453450 A>T did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr2:182360591 G>T maps to NM_000885.4 G490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr12:56086981 G>A maps to ENST00000347027 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr12:56092570 G>A maps to ENST00000347027 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr10:15701024 C>T maps to NM_003638.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr10:15634227 T>A maps to NM_003638.1 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr16:31409189 G>A maps to ENST00000444228 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr17:3649117 C>T maps to NM_002208.4 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr16:31332674 G>T maps to NM_001145808.1 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr16:31309088 T>G maps to NM_001145808.1 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr16:31373160 G>A maps to NM_000887.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr10:33209232 G>A maps to ENST00000374956 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr23:70522290 A>G did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr21:46311818 C>T maps to NM_000211.3 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr17:73733409 G>A maps to NM_001005619.1 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr3:124578104 G>C maps to NM_002213.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr12:53589941 G>A maps to NM_000889.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr13:102220074 G>A maps to NM_004791.1 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr3:52822296 C>T maps to NM_002215.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr3:52812453 C>A maps to NM_002215.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr3:52811693 C>T maps to NM_002215.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr3:52848037 G>A maps to ENST00000485816 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr10:7618968 G>C maps to ENST00000256861 Y475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr23:54785303 C>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:54784955 G>A did not map to a codon.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr23:54785125 G>T did not map to a codon.
Sequencing variant TCGA-13-1494-01A-01W-0545-08 chr5:156672998 G>A maps to NM_005546.3 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr5:156635997 G>A maps to NM_005546.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:160850970 C>A maps to NM_017625.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr1:226923899 G>A maps to NM_002221.3 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr3:4714841 A>C maps to ENST00000356617 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr3:4808380 A>G maps to ENST00000356617 P1900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr3:4816924 G>T did not map to a codon.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr3:4703821 T>A maps to ENST00000356617 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr6:33639803 A>G did not map to a codon.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr6:33636357 C>G maps to ENST00000374316 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr16:19127324 C>A maps to NM_001034841.3 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1519-01A-01W-0615-10 chr21:35257410 C>T maps to NM_003024.2 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr21:35254665 C>G maps to NM_003024.2 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:24433675 C>T maps to NM_006277.2 A1410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr1:185277997 T>A maps to NM_006469.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr1:185278529 A>T maps to NM_006469.4 C32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr1:185267295 C>G maps to NM_006469.4 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr1:185270653 G>A maps to NM_006469.4 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr1:185269233 G>A maps to NM_006469.4 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr19:49245070 G>C maps to NM_182575.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr20:10622146 C>T maps to NM_000214.2 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr3:9934739 G>A maps to NM_032492.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr1:65323362 G>A maps to NM_002227.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr9:5126736 C>T maps to NM_004972.3 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr19:17946848 G>A maps to NM_000215.3 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr5:146997487 G>A maps to NM_014790.3 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr10:133930918 C>A maps to NM_001105521.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr6:15487599 G>T maps to NM_004973.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr16:27221647 C>T maps to NM_001145348.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr20:42788454 G>A maps to NM_020433.4 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr20:42744586 G>C maps to NM_020433.4 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr14:24040580 G>A maps to NM_032452.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr14:24040670 T>A did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr19:2254189 T>A maps to NM_144616.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr23:8591674 T>C did not map to a codon.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr23:8555962 G>T did not map to a codon.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr23:8553412 T>A did not map to a codon.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr23:8522029 G>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:8503804 A>G did not map to a codon.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr3:124436216 A>T maps to NM_001024660.3 A2800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr9:712313 G>T maps to NM_015158.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:62737154 G>A maps to NM_181712.4 N669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr1:62739569 G>A maps to NM_181712.4 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr1:62740523 T>C maps to NM_181712.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr16:75663369 C>T maps to NM_001130089.1 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr18:44589401 A>G maps to ENST00000356157 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr1:15392124 G>T did not map to a codon.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr3:127682209 C>T maps to NM_207335.2 C557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr3:42727989 G>T maps to NM_152393.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:85280327 A>C maps to NM_020122.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr1:111060743 C>G maps to NM_005549.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr12:5154497 C>A maps to NM_002234.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr12:5153870 G>A maps to NM_002234.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr12:4920661 T>A maps to NM_002235.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr3:155838588 G>T maps to NM_172160.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr3:156234149 G>A maps to NM_172159.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr3:156177656 G>A maps to NM_172159.3 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr17:7827514 C>T maps to NM_004732.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr8:73849161 G>T maps to NM_004770.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr11:17793870 G>A maps to NM_001112741.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr23:48819868 G>C did not map to a codon.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr23:48819927 C>T did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr7:119915387 G>T maps to NM_012281.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr7:120372974 A>C maps to NM_012281.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr1:112329625 A>G maps to ENST00000315987 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr21:35821548 G>T maps to NM_000219.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr21:35821632 C>G maps to NM_000219.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr2:11053304 G>A maps to NM_002236.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr1:210857393 C>T maps to NM_172362.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr1:210856769 G>A maps to NM_172362.2 N941N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr17:40330943 C>T maps to NM_012285.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr14:63174534 C>T maps to NM_139318.3 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr14:63416872 C>T maps to NM_139318.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr2:163236361 C>T did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr2:163256870 G>C maps to NM_033272.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr2:96040110 G>A maps to NM_013434.4 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr4:20884249 C>T maps to ENST00000382152 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr21:39672137 A>T maps to NM_170736.1 K319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr17:68128365 C>T maps to NM_018658.1 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr2:155555787 C>T maps to NM_002239.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr14:88652211 C>T maps to NM_138318.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr14:88729713 A>C maps to NM_138318.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr2:47748837 G>A maps to NM_022055.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr14:90650587 C>T maps to NM_022054.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr6:39282849 G>C maps to NM_032115.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr1:215342540 G>T did not map to a codon.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr19:38817290 G>T maps to NM_004823.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr5:169805926 G>A maps to NM_004137.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr5:169812361 G>C maps to NM_004137.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr19:18085959 G>T maps to ENST00000222249 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr19:18092528 G>T maps to ENST00000222249 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr19:44284854 C>T maps to NM_002250.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr8:133196523 G>A maps to NM_004519.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr8:133144483 G>T maps to NM_004519.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr8:133187849 G>C maps to NM_004519.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr6:73843314 C>T maps to NM_001160133.1 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr13:50590106 C>T maps to NM_173605.1 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr8:99441337 C>T maps to NM_020697.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr1:196392243 C>A did not map to a codon.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr1:196295869 G>A maps to NM_198503.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr1:196398704 A>T did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr1:196367691 C>T did not map to a codon.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr5:143853577 G>A maps to NM_020768.3 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr22:37458585 C>T maps to ENST00000403888 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr2:201355032 C>T maps to NM_152387.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr16:67354660 G>C maps to NM_001100915.1 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr6:36449513 A>T maps to NM_173562.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr7:66104164 G>C maps to NM_153033.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr7:66103878 G>A maps to ENST00000451741 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr13:103441514 C>T maps to NM_024089.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr11:108350192 G>A maps to NM_153705.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr22:38877311 T>A maps to NM_016657.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr2:86709167 C>G maps to NM_001146688.1 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr5:137771376 G>A maps to NM_016604.3 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr19:5039896 C>T maps to NM_015015.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr9:7013852 G>A maps to NM_015061.3 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:53226113 C>T did not map to a codon.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr23:53222192 G>A did not map to a codon.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr23:53222649 G>A did not map to a codon.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr23:53230864 G>A did not map to a codon.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr23:53254004 C>G did not map to a codon.
Sequencing variant TCGA-36-1575-01A-01W-0615-10 chr23:53246445 C>T did not map to a codon.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr4:55971143 A>T maps to NM_002253.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr19:10610574 G>T maps to NM_203500.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr6:62604662 G>C maps to NM_152688.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr6:62611264 A>G maps to NM_152688.2 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr14:24906240 G>T did not map to a codon.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr14:24902053 C>T maps to NM_015299.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr9:2828778 C>A did not map to a codon.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr17:26964957 G>T maps to NM_014680.2 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr16:71954709 A>G maps to NM_014761.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr16:85667553 G>A maps to NM_014615.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr3:197408770 C>T did not map to a codon.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr6:42819928 C>T maps to NM_015349.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr14:70177694 G>A maps to NM_014734.3 *304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr6:24596165 C>A maps to NM_014809.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr1:35972211 C>A did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr16:15695883 G>A maps to NM_014647.3 H1530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr1:43891606 G>A maps to NM_015284.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr1:43913777 C>T maps to NM_015284.2 Q2299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr1:43898738 G>A maps to NM_015284.2 R995R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr12:22631294 T>G maps to ENST00000446597 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr12:22635665 A>C maps to ENST00000446597 L521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr16:27788938 G>T maps to NM_015202.2 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr16:27788289 G>T maps to NM_015202.2 V1497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr16:27720105 G>A maps to NM_015202.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr16:27642393 C>T maps to NM_015202.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr13:42385437 C>G maps to NM_015058.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr13:42407523 C>T maps to NM_015058.1 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr6:96988490 T>C maps to NM_015323.4 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr18:8819130 G>A maps to ENST00000456698 K1329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr18:8819154 G>A maps to ENST00000456698 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr10:75557649 G>T maps to NM_015037.2 G1258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr4:154502584 T>G maps to NM_001131007.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr6:84904723 G>C maps to NM_014895.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr18:29444597 G>A maps to NM_014939.3 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr18:29412045 C>T did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr18:29497612 C>A maps to NM_014939.3 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr4:123161216 T>A maps to NM_015312.3 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr4:123271113 A>G maps to NM_015312.3 E4578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr15:81173441 C>T maps to NM_018689.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr23:118223498 C>T did not map to a codon.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr23:118239037 A>T did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr23:118228014 T>A did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr23:118221701 C>A did not map to a codon.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr23:118250615 A>C did not map to a codon.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr23:118221319 C>T did not map to a codon.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr23:118220698 G>A did not map to a codon.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr4:57181695 G>C maps to NM_020722.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr4:57193864 G>A maps to NM_020722.1 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr10:24762209 C>T maps to NM_019590.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr10:70776165 G>A maps to NM_015634.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr2:97271055 C>A did not map to a codon.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr1:109714568 G>C maps to NM_020775.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr7:86522376 T>A maps to NM_001142749.2 K909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr7:86556229 T>G maps to NM_001142749.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr3:113737637 C>A maps to NM_020817.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr14:94103631 A>G maps to ENST00000393153 P1990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr14:94060162 G>A maps to ENST00000393153 W1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr14:94079194 C>T maps to ENST00000393153 D1291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1525-01A-01W-0615-10 chr8:95508083 C>T maps to NM_015496.3 L1473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr10:30315773 C>T maps to NM_020848.2 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr10:30317347 C>A maps to NM_020848.2 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr10:30336585 C>T maps to NM_020848.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr12:13221381 G>C did not map to a codon.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr18:59894531 T>G maps to NM_020854.3 L290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr18:59894634 G>T maps to NM_020854.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr9:100085203 G>C did not map to a codon.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr9:100092885 T>G maps to ENST00000375206 L887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1583-01A-01W-0615-10 chr9:100079449 G>A maps to ENST00000375206 W483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr1:180885526 G>T maps to NM_020950.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr18:43438529 C>A did not map to a codon.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr22:44692679 C>T maps to NM_001099294.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr2:176804338 T>C maps to NM_030650.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr20:36869647 G>A maps to NM_001029864.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr9:20923751 T>A maps to NM_017794.3 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr9:20988331 C>T maps to NM_017794.3 G1636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr9:20740324 T>C maps to NM_017794.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr9:20715366 C>A maps to NM_017794.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr9:20912863 G>A did not map to a codon.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr6:111587448 C>T maps to NM_153369.2 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr6:30653318 G>T maps to NM_133471.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr9:115421781 C>T maps to NM_133465.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr8:22475863 C>G maps to NM_021174.5 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr1:11983199 C>T maps to ENST00000376576 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr3:113377825 A>G maps to NM_001009899.2 H901H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr23:73963679 C>A did not map to a codon.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr23:73959988 T>C did not map to a codon.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr23:73965419 C>T did not map to a codon.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr23:73963171 G>T did not map to a codon.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr23:73960359 G>T did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr23:73960334 T>C did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:73960160 C>G did not map to a codon.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr23:73961169 C>T did not map to a codon.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr2:8926116 G>T maps to NM_020738.2 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr2:8926462 T>C maps to NM_020738.2 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr2:8940568 C>T maps to NM_020738.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr9:116854182 A>G maps to ENST00000259410 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr6:17834245 T>C maps to NM_022113.4 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr20:16496270 T>A maps to NM_024704.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1348-01A-01W-0494-09 chr1:21016708 C>T maps to NM_020816.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1575-01A-01W-0615-10 chr1:21014309 C>T maps to NM_020816.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr17:43003537 G>A maps to ENST00000438933 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr1:10425304 T>C did not map to a codon.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr1:10403308 C>T maps to ENST00000377086 R1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr17:4923835 G>A maps to NM_006612.5 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr10:91479225 T>C maps to ENST00000416354 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr12:39726177 T>C maps to ENST00000395670 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr12:39695436 C>A maps to ENST00000395670 V1593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr12:39734076 T>A maps to ENST00000395670 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:200959144 G>C maps to NM_017596.2 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr9:34257951 C>T maps to NM_194313.2 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr1:245704146 C>T maps to NM_018012.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr9:86518418 T>G maps to NM_017576.1 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr5:61668333 C>T maps to NM_001098511.1 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr17:51902167 C>T maps to NM_032559.4 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr20:30914649 G>T maps to NM_004798.3 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr2:26203451 G>T maps to NM_002254.6 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr2:26177254 C>T did not map to a codon.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr23:69510632 A>T did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:69573488 A>G did not map to a codon.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr23:69563731 A>C did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr23:69626848 G>A did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr12:57965902 A>G maps to NM_004984.2 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr15:90188642 G>A maps to NM_198525.2 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr8:145694903 A>C maps to NM_145754.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr19:55250042 T>A maps to NM_015868.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:158061245 C>T maps to ENST00000368173 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr1:158064748 C>T maps to ENST00000368173 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr19:36351229 A>G maps to NM_199180.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr11:126306736 G>A maps to NM_032531.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr1:204161956 G>T maps to ENST00000306118 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr4:55573315 C>T maps to NM_000222.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr4:55602953 G>A maps to NM_000222.2 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr4:55593643 C>A maps to NM_000222.2 Y570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr4:39450110 A>G maps to NM_175737.3 Q980Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr4:39439522 G>T maps to NM_175737.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr2:10188450 C>T maps to NM_003597.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr23:56291711 G>A did not map to a codon.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr14:50244913 G>A maps to NM_014315.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr6:42988452 C>T maps to NM_057161.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr1:205312381 G>C maps to NM_018203.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:117054277 C>A did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:117035835 G>A did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:24006143 C>T did not map to a codon.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr1:173743506 G>C maps to NM_014458.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr6:53518998 G>A maps to NM_001003760.4 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr6:97533045 C>T maps to NM_052904.3 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr23:21674168 T>G did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:86873048 C>A did not map to a codon.
Sequencing variant TCGA-24-1603-01A-01W-0551-08 chr23:86888774 T>A did not map to a codon.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr3:183273207 C>T maps to NM_130446.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr9:21333995 G>C maps to NM_018847.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr9:21333628 A>G maps to NM_018847.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr19:51527574 G>T maps to NM_001167605.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr19:51534151 G>A maps to NM_019598.2 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr19:51361527 C>A maps to NM_001648.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr19:51480920 G>T maps to NM_005046.2 C211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr4:187177215 C>A maps to ENST00000511608 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr2:48722867 C>T maps to NM_001135629.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr2:48687277 T>G maps to NM_001135629.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr2:48701860 G>C maps to NM_001135629.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1659-01B-01W-0615-10 chr12:10588461 C>A maps to NM_002260.3 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr12:10570981 G>A maps to NM_007333.2 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr1:241755349 C>A maps to NM_003679.3 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr10:135020390 G>T maps to ENST00000368572 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr12:123057756 C>A maps to NM_014708.4 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr12:123047186 G>A maps to NM_014708.4 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0891-01A-01W-0420-08 chr12:123087764 C>T maps to NM_014708.4 I1692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr12:123014648 C>T maps to NM_014708.4 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr6:117010540 C>T maps to NM_002269.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr6:117046966 A>C maps to NM_002269.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr17:45734426 G>C did not map to a codon.
Sequencing variant TCGA-09-1659-01B-01W-0615-10 chr1:152732147 C>T maps to NM_001025231.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr1:152732621 C>T maps to NM_001025231.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr7:91865842 G>T maps to NM_194456.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr17:39019538 C>G maps to NM_000223.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr17:39658837 C>G maps to NM_153490.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr17:39739811 C>T maps to NM_000526.4 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr17:39780466 G>A maps to NM_000422.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr17:39777277 G>A maps to NM_000422.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr12:53045434 G>A maps to NM_000423.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr12:53039024 G>A maps to NM_000423.2 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr12:53045404 C>T maps to NM_000423.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr17:39081621 C>A maps to NM_015515.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr17:39553626 G>A maps to ENST00000393998 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr17:39645948 G>T maps to NM_003771.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr17:39644652 T>A did not map to a codon.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr17:39595592 G>C maps to NM_006771.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr12:53201602 C>A maps to NM_002272.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr12:53207428 G>A maps to NM_002272.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr12:53202598 C>T maps to NM_002272.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr12:52882326 G>A maps to NM_005554.3 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr12:52863577 G>A maps to NM_173086.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr12:52865202 A>G did not map to a codon.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr12:52992857 G>T maps to NM_080747.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr12:53012143 C>G maps to NM_175068.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr12:52962017 G>A maps to NM_175053.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr12:53170616 C>T maps to NM_015848.4 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr12:53238392 C>A maps to NM_173352.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr12:53224024 C>G maps to NM_175834.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr12:53293651 G>A maps to NM_002273.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr12:52699058 C>A maps to NM_002284.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr21:46066407 C>T maps to NM_198692.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr21:46047293 C>G maps to NM_198690.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr21:31803039 A>G maps to NM_181600.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1525-01A-01W-0615-10 chr21:31869269 G>A maps to NM_181610.1 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr11:1629564 A>G maps to NM_001012708.2 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr11:1643005 G>A maps to ENST00000359229 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr21:31986187 G>T maps to NM_181602.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr12:118198937 C>T maps to ENST00000339824 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr3:119205678 G>C did not map to a codon.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr3:134339675 G>A maps to NM_178554.4 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr23:153130287 T>G did not map to a codon.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr23:153129864 C>T did not map to a codon.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr23:153130950 G>A did not map to a codon.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr23:153130773 G>T did not map to a codon.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr23:153131182 G>C did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:153130811 G>T did not map to a codon.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr23:153129913 G>A did not map to a codon.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr23:153130575 C>T did not map to a codon.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr23:153136543 G>A did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr23:153130953 A>C did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr20:42143411 G>A maps to NM_032107.4 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr22:41605746 G>A maps to NM_031488.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr6:130376383 G>A maps to NM_032438.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr6:130413936 A>G maps to NM_032438.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr8:71553241 T>C maps to NM_016027.2 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr12:6883998 C>T maps to NM_002286.5 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr19:54871662 C>T maps to NM_002287.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr19:55019331 T>C maps to NM_002288.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr18:6999479 C>A maps to NM_005559.2 E1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr18:6986306 G>A maps to NM_005559.2 Y1736Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr18:7013921 G>A maps to NM_005559.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr18:7050778 T>G maps to NM_005559.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr6:129826343 G>T did not map to a codon.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr6:129663609 C>T maps to NM_000426.3 N1478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr18:21419835 C>G maps to ENST00000416669 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr6:112462024 A>G maps to NM_001105206.1 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr6:112506503 G>A maps to NM_001105206.1 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr6:112443317 G>A maps to NM_001105206.1 H1458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr7:107638874 G>A maps to NM_002291.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1574-01A-01W-0615-10 chr3:49169730 C>A maps to NM_002292.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr1:209790789 C>A maps to NM_000228.2 E1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr1:183195830 A>C did not map to a codon.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr9:133963008 G>T maps to ENST00000355048 R1471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr9:133936539 C>A maps to ENST00000355048 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr23:119582823 C>A did not map to a codon.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr3:182870291 C>G did not map to a codon.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr7:55467797 G>A did not map to a codon.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr7:55459484 G>C did not map to a codon.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr22:33700282 G>A maps to NM_133642.3 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr5:154182973 G>T did not map to a codon.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr4:113571626 G>A maps to ENST00000509061 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr5:145529205 A>T maps to NM_020117.9 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr3:45518042 C>T maps to NM_015340.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr23:64738126 T>C did not map to a codon.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr23:64744050 C>G did not map to a codon.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr23:64743483 G>A did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:64749715 C>G did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr15:101024821 C>A maps to ENST00000394113 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr15:101019637 T>A maps to ENST00000394113 K182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr19:8322866 C>A maps to NM_024552.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr6:150004238 T>C maps to NM_004690.2 K662K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr13:21553913 C>T maps to NM_014572.2 W896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr1:225598019 G>C maps to NM_194442.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr15:68118525 C>T maps to ENST00000380035 R120R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-61-2614-01A-01W-1092-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr1:152799995 C>T maps to NM_178348.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr1:152659648 C>T maps to NM_014357.4 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr1:152648664 C>A maps to NM_178429.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr1:152595321 C>T maps to NM_178431.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr1:152538648 G>T maps to NM_178435.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr1:32745785 C>T maps to ENST00000373562 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr9:138557548 C>T maps to ENST00000277526 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr10:98714824 A>T maps to NM_001170765.1 K150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr13:46716515 C>T maps to NM_002298.4 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr13:46732675 G>T maps to NM_002298.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr2:136594680 G>T maps to NM_002299.2 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1325-01A-01W-0490-10 chr2:136566474 G>A maps to NM_002299.2 Q1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr10:88451685 C>T maps to NM_001171610.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr10:88441362 G>C maps to NM_001171610.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr10:88459049 G>T maps to NM_001171611.1 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr11:18485527 C>T maps to NM_144972.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr11:18472563 C>A maps to NM_017448.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr19:11213433 C>A maps to NM_000527.4 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:25880416 G>T maps to NM_015627.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr22:44893391 T>C maps to NM_032287.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr4:109086251 C>A did not map to a codon.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr1:153177461 C>T maps to NM_001010857.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr19:54660763 C>T did not map to a codon.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr1:66101913 C>G maps to NM_002303.5 S905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr1:43223531 G>A maps to NM_022356.3 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr3:189838070 G>C maps to NM_018192.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr11:63276300 C>A maps to NM_001142535.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr19:40095961 C>T maps to NM_013268.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr19:39292787 G>T maps to NM_006149.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr17:25974316 T>G maps to NM_009587.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr1:202275995 C>T maps to NM_001017403.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr1:202287878 G>T maps to NM_001017403.1 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr19:49519471 C>T maps to NM_000894.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr7:103969406 G>A maps to NM_199000.2 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr3:9594306 C>G maps to NM_198560.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr17:35297670 C>T maps to NM_005568.3 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr17:35300289 G>T maps to NM_005568.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr1:180241139 A>T maps to NM_033343.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr1:75626510 A>C maps to NM_001001933.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr19:48638977 C>T maps to NM_000234.1 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr17:33313064 G>A maps to NM_013975.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr19:55106415 A>T maps to NM_006863.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr19:54803580 G>T maps to ENST00000251375 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr19:54849489 G>A maps to NM_012276.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr19:54848238 G>A maps to NM_012276.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr19:55143563 C>T maps to ENST00000427581 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr19:54724539 G>A maps to NM_001081450.1 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr19:55179358 C>T maps to ENST00000391733 Y413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr19:55179202 A>T maps to ENST00000391733 K388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr19:54756851 T>C did not map to a codon.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr22:31658652 C>T maps to NM_001031801.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr12:81205335 G>A maps to NM_004664.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr1:226474092 T>A maps to ENST00000366807 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr15:58830575 C>T maps to NM_000236.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr10:90492015 C>T maps to NM_001080518.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr1:145492368 T>A maps to NM_153713.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr17:18141443 C>T maps to NM_004140.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr17:18138571 C>A maps to NM_004140.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr5:36104192 T>G maps to NM_001007527.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr5:36123027 G>A maps to NM_001007527.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2355-01A-01W-0799-08 chr19:2432479 C>T maps to NM_032737.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr3:69171390 G>C maps to NM_198271.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr3:69158248 C>T maps to NM_198271.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:97833388 G>A maps to NM_014916.3 T1458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr5:96314939 G>T maps to NM_005575.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1603-01A-01W-0551-08 chr5:96328795 T>C maps to NM_005575.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr4:54347946 G>A maps to NM_001126328.1 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr4:54424123 C>T maps to NM_032622.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr9:90747150 C>T maps to NM_001166137.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr16:20824600 C>G maps to NM_030941.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr19:5707746 G>A maps to NM_004793.2 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr19:5711913 C>T maps to NM_004793.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr2:100916304 C>A maps to NM_198461.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr23:118145900 A>G did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr23:118143137 T>A did not map to a codon.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr8:23174540 C>T maps to NM_002318.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr10:100011328 G>A maps to NM_032211.6 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr10:100017746 G>A maps to NM_032211.6 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr6:161010634 G>T maps to NM_005577.2 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr6:161027641 A>C maps to NM_005577.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr6:161015015 C>T maps to NM_005577.2 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr9:113637931 G>A maps to NM_057159.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr1:85279813 C>T maps to NM_012152.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr23:78010949 G>A did not map to a codon.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr23:78011284 G>C did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr23:78011284 G>T did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:78010925 C>A did not map to a codon.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr12:6730186 G>A maps to ENST00000435659 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr5:1479750 G>A maps to NM_024830.3 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr2:11905846 C>G maps to ENST00000396099 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr20:39987134 C>T maps to NM_022896.1 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr1:99772184 G>T maps to NM_014839.4 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr1:99772256 C>T maps to NM_014839.4 Y661Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr4:151242514 T>A maps to NM_006726.3 P2497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:114404899 T>C did not map to a codon.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr23:114347847 T>A did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr23:114404878 T>C did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:114418980 A>C did not map to a codon.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr23:114414016 G>A did not map to a codon.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr19:39804671 C>T maps to NM_020862.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr6:40400039 G>T maps to NM_020737.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr6:40360134 G>T maps to NM_020737.1 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr19:36435578 C>T maps to NM_024509.1 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr14:42373366 G>T maps to NM_152447.3 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr14:42356271 C>A maps to NM_152447.3 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr3:66436453 G>A maps to NM_015541.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr3:66434544 G>T maps to NM_015541.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr1:113641325 G>A did not map to a codon.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr1:113657286 G>A maps to NM_014813.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr10:85981798 G>A maps to NM_001017924.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr10:85981765 A>G maps to NM_001017924.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr12:25257308 C>G maps to ENST00000354454 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr12:57602962 G>T maps to NM_002332.2 V4081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr12:57552344 C>A maps to NM_002332.2 Y574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr12:57584599 G>A maps to NM_002332.2 W2348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr12:57578927 C>T maps to NM_002332.2 R2135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr12:57594907 C>T maps to NM_002332.2 C3439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr2:141200192 C>T did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr2:141294204 G>T maps to NM_018557.2 T2529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr2:141660723 C>G maps to NM_018557.2 S1177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr2:169989188 C>G maps to NM_004525.2 V4541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr2:169985520 A>T did not map to a codon.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr2:169993964 T>A maps to NM_004525.2 I4519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr2:170062939 A>G maps to NM_004525.2 S2430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr19:33696380 C>T maps to NM_002333.3 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr11:46893149 C>A maps to ENST00000256991 E1585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr12:12311940 G>T maps to NM_002336.2 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr12:12397427 C>A maps to NM_002336.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr2:44171016 C>T maps to NM_133259.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr6:53660121 C>A maps to NM_018214.4 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr6:25517616 T>C maps to NM_017640.5 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr14:24531754 C>G maps to NM_138360.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr7:102579997 C>T maps to NM_001031692.2 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr3:46586714 C>A maps to NM_024512.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1558-01A-01W-0615-10 chr10:134175055 G>A maps to NM_030626.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr18:7231562 G>T maps to NM_001105581.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr18:7232017 C>A maps to NM_001105581.1 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr3:196387725 G>C maps to NM_198565.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr17:30376235 A>G maps to ENST00000327564 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr1:100618067 G>A maps to NM_144620.2 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr1:100626045 C>T maps to NM_144620.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr1:70650575 G>C maps to NM_017768.4 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr1:46752172 T>A did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr11:40136252 A>T maps to NM_020929.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr11:40137797 A>C maps to NM_020929.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr11:40136957 C>T maps to NM_020929.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr16:84203519 G>A maps to NM_178452.4 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr1:165513562 G>T maps to NM_001005214.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr1:165532889 C>T maps to NM_001005214.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr3:120054736 C>T maps to NM_001099678.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr3:120053754 A>C maps to NM_001099678.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr4:52860769 G>C maps to NM_001024611.1 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr1:70541779 G>A maps to NM_020794.2 T1379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr1:90048316 G>T maps to NM_015350.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr1:90180459 G>C maps to NM_032270.4 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr1:90400054 G>C maps to NM_001134479.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr19:7965233 A>G maps to NM_025061.3 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr8:86047173 T>G maps to NM_033402.4 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr3:37125234 G>A maps to NM_006309.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr3:37190396 G>A maps to NM_006309.2 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr12:85518018 T>C maps to NM_001079910.1 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr12:85449555 C>T maps to NM_001079910.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr12:85438508 A>G maps to NM_001079910.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr1:74648284 A>G maps to NM_001105659.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr15:101595397 G>A maps to NM_024652.3 E1434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1571-01A-01W-0615-10 chr12:40699633 C>G maps to NM_198578.3 V1275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr12:40728866 G>A maps to NM_198578.3 K1952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr7:110762875 C>T maps to NM_018334.4 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr7:110763550 C>T maps to NM_018334.4 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr2:80530191 C>A maps to NM_178839.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr2:80529618 C>A maps to NM_178839.4 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr5:138209535 C>T maps to NM_015564.2 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr9:130230080 T>G maps to NM_001005374.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr9:130230080 T>G maps to NM_001005374.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr17:42141261 G>T maps to ENST00000411445 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr3:14239603 G>T maps to NM_014463.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr19:35757274 C>T maps to NM_205834.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr6:31541151 G>C maps to NM_000595.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr14:24779908 G>A maps to ENST00000336557 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr2:33413785 C>T maps to ENST00000354476 Y523Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr19:41115541 C>G maps to ENST00000308370 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr6:144167243 C>T maps to NM_032860.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:23418180 C>T maps to NM_001142546.1 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr1:23419338 T>G maps to NM_001142546.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr23:114524415 G>T did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:114537921 A>T did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr6:31675349 C>A maps to ENST00000375834 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr6:31678361 C>T maps to NM_001003693.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr4:4285445 T>G maps to NM_017816.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr2:99861868 A>C maps to NM_175735.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr8:56866544 T>G did not map to a codon.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr19:42341282 T>G maps to NM_173506.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr2:150061919 T>G did not map to a codon.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr8:54963652 C>A maps to ENST00000419058 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr1:151134351 A>T maps to NM_212551.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr1:235897869 C>T maps to NM_000081.2 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr22:21344672 A>C did not map to a codon.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr22:21343122 C>T maps to NM_006767.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr4:151505206 C>A maps to NM_006439.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr20:15948270 C>G maps to ENST00000310348 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr7:2255793 C>A maps to NM_003550.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr11:47345814 G>T did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:152482177 T>A did not map to a codon.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr23:151092856 G>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:151092587 T>A did not map to a codon.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr23:30268729 C>G did not map to a codon.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr23:30269046 T>A did not map to a codon.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr23:35820615 T>A did not map to a codon.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr23:35820779 T>G did not map to a codon.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr23:30236763 C>T did not map to a codon.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr23:30254352 G>T did not map to a codon.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr23:30254668 G>T did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr23:30261145 T>C did not map to a codon.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr23:30261038 A>C did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr23:26212647 T>A did not map to a codon.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr23:26212099 G>A did not map to a codon.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr23:26212379 C>A did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:26212987 T>C did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr23:26212168 C>T did not map to a codon.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr23:140995758 T>A did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr23:140994935 G>T did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:140994025 C>A did not map to a codon.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr23:140996465 G>A did not map to a codon.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr23:141291063 A>G did not map to a codon.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr23:141291396 G>C did not map to a codon.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr23:140984667 A>G did not map to a codon.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr23:51637765 C>A did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr23:51639605 G>A did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:51638325 A>T did not map to a codon.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr23:51639635 C>G did not map to a codon.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr23:51644797 G>A did not map to a codon.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr23:54841099 G>C did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:54836165 A>T did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:54839592 G>T did not map to a codon.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr23:54836542 C>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:75650184 T>C did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:75650480 G>C did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:75649201 C>A did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr3:184428928 C>T maps to NM_022149.4 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr3:184429409 A>T maps to NM_022149.4 L67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr23:55479306 C>T did not map to a codon.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr7:77885425 C>G maps to NM_012301.3 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr7:77789396 G>T maps to NM_012301.3 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr7:77756639 C>T maps to NM_012301.3 R1099R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr23:77112370 C>A did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr8:120252478 G>C maps to ENST00000276681 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr18:56414869 C>T maps to NM_006785.2 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr18:56390337 C>T maps to NM_006785.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr5:179200914 C>A maps to NM_014757.4 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr23:149639720 C>T did not map to a codon.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr1:118039452 G>T maps to NM_006699.3 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr1:26079973 G>T did not map to a codon.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr15:91448686 G>A maps to NM_006122.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr19:12774202 C>A maps to NM_000528.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr15:75654985 G>A maps to NM_006715.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1348-01A-01W-0494-09 chr23:43572006 C>A did not map to a codon.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr23:43652773 A>T did not map to a codon.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr15:43818599 G>A maps to ENST00000382031 G1881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr15:43818725 C>A maps to ENST00000382031 G1923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr5:71490039 C>T maps to NM_005909.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr5:71490933 A>G maps to NM_005909.3 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr19:17836855 G>A maps to NM_018174.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr2:210560574 T>A maps to NM_002374.3 S1227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr2:210518127 G>A maps to NM_002374.3 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr2:210558771 C>G maps to NM_002374.3 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr2:210570347 A>G maps to NM_002374.3 R1543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr2:210569214 A>T maps to NM_001039538.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr17:11984781 C>T maps to ENST00000415385 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr3:185165691 G>T maps to NM_004721.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:19390892 C>A did not map to a codon.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr23:19380929 T>C did not map to a codon.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr23:19380951 C>G did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:19410173 A>T did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr6:137019625 C>G did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr6:136934307 C>A maps to NM_005923.3 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr1:27690831 C>G maps to NM_004672.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr14:71275546 G>A maps to NM_033141.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr11:64557095 T>C maps to NM_004579.2 R792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr2:39485579 A>G maps to NM_003618.2 C793C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr1:36641854 G>A maps to NM_018067.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:20028955 G>A did not map to a codon.
Sequencing variant TCGA-13-0889-01A-01W-0419-10 chr23:20043111 C>T did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr23:135302949 G>T did not map to a codon.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr23:135326816 T>A did not map to a codon.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr22:22160201 A>T maps to NM_138957.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr22:22160159 G>C maps to NM_138957.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr22:50693770 C>T maps to NM_002969.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr6:35995963 G>C maps to NM_139012.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr12:112318332 T>A did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr15:42107467 G>A maps to NM_001128608.1 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr18:32677555 G>T did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr2:27245109 A>G maps to NM_012326.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr2:27248875 C>T maps to NM_012326.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr4:164534464 C>T did not map to a codon.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr17:60837259 C>T maps to NM_152598.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr5:126213924 C>G maps to NM_178450.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr5:10415675 T>G maps to NM_005885.2 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr1:32800409 G>A maps to NM_023009.5 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr2:119729102 C>G maps to NM_006770.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr2:119699962 C>T maps to NM_006770.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr1:220808803 C>G maps to NM_018650.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr5:68728872 C>T maps to NM_001038603.2 L486L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-29-1691-01A-01W-0633-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr6:29454575 A>T maps to NM_052967.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr6:29455288 A>G maps to NM_052967.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr3:186974475 C>A maps to NM_139125.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr3:186954119 C>T maps to NM_139125.3 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr3:186969526 T>C maps to NM_139125.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr19:12958126 C>T maps to NM_014975.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr1:46501737 G>C maps to NM_015112.2 *1799Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:46489461 G>T maps to NM_015112.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr5:66448675 A>T maps to NM_001164664.1 T1169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr1:31187154 G>T maps to NM_002379.3 C460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr1:31191761 G>A maps to NM_002379.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr8:99039927 G>T maps to ENST00000254898 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr20:3838322 C>T maps to NM_020746.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr20:3845436 T>G did not map to a codon.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr18:47803284 C>T maps to ENST00000424334 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr3:129155580 C>G maps to NM_003925.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr2:149247805 A>C maps to ENST00000404807 G1535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr2:149260042 G>A maps to ENST00000404807 L1667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2409-01A-01W-0799-08 chr12:57919794 C>G maps to NM_052897.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr10:54531251 G>T maps to NM_000242.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr3:152018064 C>G maps to NM_021038.3 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:131525092 G>A did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr6:20151416 T>A maps to NM_001080480.1 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr17:49270164 T>C maps to ENST00000389496 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr16:84115431 G>C maps to NM_003791.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr23:21861407 C>T did not map to a codon.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr18:13884638 G>A maps to NM_000529.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr20:54824012 C>T maps to ENST00000371389 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr18:13826420 C>T maps to NM_005913.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr18:13826570 C>T maps to NM_005913.2 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr9:37888378 G>A maps to NM_033412.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr9:37888028 A>G maps to NM_033412.3 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr5:112630025 C>T maps to NM_002387.2 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr3:182755054 G>A maps to NM_020166.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr5:70900296 T>C did not map to a codon.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr2:71351485 C>T maps to NM_032601.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:138669903 C>A did not map to a codon.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr23:138695387 T>C did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:138698501 A>T did not map to a codon.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr6:100390993 G>A maps to NM_032503.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr3:127325075 C>A maps to NM_004526.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr6:52143647 C>T maps to ENST00000419835 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr2:136627909 C>G maps to NM_005915.4 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr1:85397197 A>G maps to NM_153259.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr5:94046532 G>C maps to NM_024717.4 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr23:119746082 A>T did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr6:30671315 T>C did not map to a codon.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr14:47389223 G>T maps to NM_001113498.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:207613840 T>C maps to NM_001039845.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1626-01A-01W-0615-10 chr2:207625681 T>C maps to NM_001039845.1 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr12:68720730 A>C maps to NM_017440.4 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr1:204515956 G>A maps to NM_002393.3 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr6:90371844 A>G maps to NM_014611.1 G4842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr6:90368336 G>A maps to NM_014611.1 Q5005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr6:84061797 T>C maps to NM_002395.4 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2350-01A-01W-0799-08 chr11:86152476 G>A maps to NM_001014811.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr1:29522724 G>A maps to NM_016011.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr23:70352802 C>G did not map to a codon.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr3:151105722 C>T maps to NM_053002.4 Y1703Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr3:150911296 A>G maps to NM_053002.4 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr12:116406746 G>T maps to NM_015335.4 R2075R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr23:40540084 A>T did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:40540155 T>C did not map to a codon.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr9:136211029 G>A maps to NM_133640.3 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr6:131917303 C>G did not map to a codon.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr17:38186111 G>T maps to NM_014815.3 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr19:50331741 C>T maps to NM_030973.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr19:16687872 C>A maps to NM_004831.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr5:88027629 G>T maps to NM_002397.4 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr5:126758359 A>T did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr5:126770394 T>C maps to NM_032446.2 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1583-01A-01W-0615-10 chr5:126755841 C>T maps to NM_032446.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr19:42839281 G>A maps to ENST00000251268 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr22:42172134 A>C maps to NM_152513.3 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr10:15008562 T>A maps to NM_001080836.2 Y32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr7:15725598 C>A maps to NM_005924.4 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr6:46761418 T>C maps to NM_005588.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr7:100028199 C>T maps to NM_019606.5 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr15:90320118 G>A maps to NM_001039958.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr7:130138006 C>T maps to NM_002402.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr17:2323626 G>A maps to NM_024086.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr14:21464690 G>A maps to NM_001029991.1 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr11:28232745 G>A did not map to a codon.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr9:132397559 C>T maps to NM_014064.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr1:171765791 C>T maps to NM_015935.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr4:119618342 A>G maps to NM_020961.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr17:74763466 G>C did not map to a codon.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr15:42035077 C>T maps to ENST00000219905 V1689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr7:141759304 C>A maps to ENST00000475668 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr5:180219791 G>A maps to NM_001114617.1 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr12:86373821 G>A maps to ENST00000393205 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr12:86377376 G>A maps to ENST00000393205 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr2:135012007 C>T maps to NM_002410.3 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:88423914 A>G maps to NM_152706.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr7:88424241 G>A maps to NM_152706.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr5:43280530 C>T maps to NM_153361.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr5:43277225 A>C maps to NM_153361.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr10:103546266 C>A maps to NM_012215.3 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr10:131506260 C>T maps to NM_002412.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr1:222827729 G>C did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr1:222838885 C>T maps to NM_198551.2 G1883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr23:10437841 C>G did not map to a codon.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr23:10463676 C>G did not map to a codon.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr23:107084207 C>T did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:107097869 T>A did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr23:107084582 G>A did not map to a codon.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr19:1257189 C>T maps to NM_177401.4 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr1:67411869 A>G maps to NM_001077700.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr19:334515 G>A maps to NM_017550.1 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr17:73263912 G>A maps to NM_020679.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr1:12089945 C>T maps to NM_021933.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr17:4799852 C>T maps to NM_153827.4 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr13:24443440 A>G maps to NM_005932.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr3:69928326 C>T maps to ENST00000448226 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr10:129907444 G>A maps to NM_002417.4 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr7:131084025 T>A maps to NM_013255.4 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr1:47048939 C>A maps to NM_003684.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:47034134 A>G maps to NM_003684.4 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr15:23811057 T>C maps to NM_005664.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1571-01A-01W-0615-10 chr15:23811186 G>A maps to NM_005664.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr15:23811153 C>T maps to NM_005664.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr17:56283477 G>A maps to NM_017777.3 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr4:185616498 G>C maps to NM_024629.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr3:37042535 C>T maps to NM_000249.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr3:37061950 C>G maps to NM_000249.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr12:49427468 A>T maps to NM_003482.3 L3673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr12:49437652 G>A maps to NM_003482.3 Q1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr12:49432060 G>A maps to NM_003482.3 G3026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr7:151859420 G>A maps to ENST00000355193 N3747N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr7:151851205 G>A maps to ENST00000355193 I4112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr7:151851442 G>A maps to ENST00000355193 S4073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr7:151843820 C>G did not map to a codon.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr7:151917706 T>A maps to ENST00000355193 K1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr19:36223566 G>T maps to NM_014727.1 V2039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1771-01A-01W-0633-09 chr19:36218513 C>G maps to NM_014727.1 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr10:22023049 G>A maps to NM_004641.3 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr6:168352357 A>T maps to ENST00000400822 R1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr3:154834717 C>G maps to NM_007289.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr1:2528035 G>A maps to NM_033467.3 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr1:2525355 G>A maps to NM_033467.3 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr8:89128917 T>A maps to NM_005941.4 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr8:89128810 G>A maps to NM_005941.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr16:55532289 C>A maps to NM_004530.4 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr16:55532237 G>A maps to NM_004530.4 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr16:55523683 G>A maps to NM_004530.4 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr16:55532303 C>T maps to NM_004530.4 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr11:102567489 G>A maps to NM_022122.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0968-01A-01W-0484-10 chr20:44637669 G>C maps to NM_004994.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr20:44639842 G>A maps to NM_004994.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr4:90816311 G>T maps to NM_007351.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr4:90874313 A>G maps to NM_007351.2 V1144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr14:61285489 A>G maps to NM_002431.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr9:27455161 G>A maps to NM_024761.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr6:29638161 C>T maps to NM_002433.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr3:108773722 G>A maps to NM_014429.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr3:108822694 C>A did not map to a codon.
Sequencing variant TCGA-36-1569-01A-01W-0615-10 chr3:108724096 G>A maps to NM_014429.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr22:31330112 C>T maps to ENST00000397641 E753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr23:106205287 T>A did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr23:106229430 C>T did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:102931233 T>G did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr8:57025500 T>A maps to NM_005372.1 *347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr23:134033375 C>T did not map to a codon.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:14929503 C>A did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr7:100212802 C>G maps to NM_023948.4 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr1:113232555 G>A maps to NM_020963.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr22:50555735 G>A maps to NM_018995.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr6:132645225 A>G maps to NM_015529.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr9:13188815 C>A maps to ENST00000319217 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr16:135505 C>G maps to NM_002434.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr15:75188493 G>A maps to NM_002435.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr17:56351008 G>A maps to ENST00000340482 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr23:154020119 T>A did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:154012324 C>G did not map to a codon.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr23:154020057 A>C did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr17:41959846 C>T maps to NM_005374.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr2:202539983 C>A maps to NM_033066.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr18:11886920 G>A maps to ENST00000344987 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr10:18112236 T>A maps to NM_002438.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr11:94192748 T>C did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr11:19077484 G>A maps to NM_054030.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr18:48327832 C>T maps to NM_001127176.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr6:160212128 G>C maps to NM_014161.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr16:418369 C>T maps to NM_006428.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr12:93881353 G>T maps to NM_172177.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:95753173 G>A maps to NM_031902.3 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr9:125033217 C>T maps to NM_138777.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr11:10651172 C>T maps to NM_001098579.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr11:60230494 G>T maps to NM_152866.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1428-01A-01W-0549-09 chr11:60559754 C>A maps to NM_206893.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr11:60170524 T>C maps to NM_032597.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr11:59828788 G>T maps to NM_006138.4 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr11:60161282 A>T maps to NM_206939.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr11:60470942 C>G maps to NM_031457.1 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr2:47657030 G>A maps to NM_000251.1 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr1:76355051 G>T maps to NM_002440.2 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr1:76276395 T>G maps to NM_002440.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr6:31727722 A>G maps to ENST00000375742 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr6:31715209 G>T did not map to a codon.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr2:48028253 C>G maps to NM_000179.2 Y1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr2:48027467 C>G maps to NM_000179.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:11781905 C>T did not map to a codon.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr10:51562387 A>G maps to NM_002443.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:64949369 A>C did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr8:15967727 C>T did not map to a codon.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr3:49934991 C>A maps to NM_002447.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr23:131207037 C>T did not map to a codon.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr23:131207038 G>A did not map to a codon.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr23:131188770 T>G did not map to a codon.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:190926977 C>A maps to NM_005259.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr16:56602818 C>G maps to NM_032935.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr11:62364297 C>G did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr8:121531005 T>C maps to NM_022045.3 C853C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr23:154293933 T>C did not map to a codon.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr7:91503498 G>C maps to NM_006980.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr8:97251754 T>C maps to NM_015942.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr13:28011387 C>A maps to NM_152912.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr23:149809888 C>T did not map to a codon.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr23:149901047 C>T did not map to a codon.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr23:149905818 T>A did not map to a codon.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr5:32263286 C>A maps to NM_001040446.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr5:32243640 C>T maps to NM_001040446.1 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr22:30416521 C>T maps to NM_021090.3 C958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr13:25823557 C>A maps to NM_004685.3 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr23:63574683 G>T did not map to a codon.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr23:63574697 T>A did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:63551598 G>T did not map to a codon.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr23:63576112 C>G did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr11:92714700 C>T maps to NM_005959.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr6:74191779 C>A maps to NM_001123226.1 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr10:30629241 C>T maps to ENST00000358107 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr10:30629202 C>T maps to ENST00000358107 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr1:237015826 T>C maps to NM_000254.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr5:7891482 A>G did not map to a codon.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr8:125565382 A>C maps to NM_014751.4 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr4:100540208 G>T maps to ENST00000511045 E793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr4:100516040 G>T did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr8:17612587 G>A maps to NM_001001924.2 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1558-01A-01W-0615-10 chr11:26584678 G>A maps to NM_001135091.1 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr19:9087710 A>T maps to NM_024690.2 P1368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr19:9089321 C>T maps to NM_024690.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr19:9087848 G>T maps to NM_024690.2 T1322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr19:8998701 G>A maps to NM_024690.2 P13627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr19:8993502 G>T maps to NM_024690.2 C13862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr19:8976816 G>A maps to NM_024690.2 I14083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr19:9085169 T>C maps to NM_024690.2 T2215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1325-01A-01W-0490-10 chr19:9073805 G>C maps to NM_024690.2 S4547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr19:9069559 G>A maps to NM_024690.2 T5962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr19:9074908 T>C maps to NM_024690.2 Q4179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr19:9086727 G>C maps to NM_024690.2 S1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr19:9077659 C>A maps to NM_024690.2 L3262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr7:100676760 T>C maps to NM_001040105.1 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr7:100681590 C>A maps to NM_001040105.1 T2298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr7:100682334 G>A maps to NM_001040105.1 V2546V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr7:100686996 A>C maps to NM_001040105.1 T4100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr7:100663430 G>A maps to NM_001040105.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr7:100686036 C>T maps to NM_001040105.1 Y3780Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr7:100696300 G>T maps to NM_001040105.1 E4380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr7:100685236 G>T maps to NM_001040105.1 E3514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr7:100678299 T>A maps to NM_001040105.1 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr7:100686897 T>G maps to NM_001040105.1 P4067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr7:100684245 C>A maps to NM_001040105.1 T3183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr7:100683891 C>G maps to NM_001040105.1 T3065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr7:100686156 C>A maps to NM_001040105.1 L3820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr7:100684113 T>A maps to NM_001040105.1 S3139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr11:1263794 C>G maps to ENST00000447027 A1898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr11:1016959 G>T maps to NM_005961.2 T1947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr4:71346826 A>G maps to NM_152291.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr4:71346631 G>A maps to NM_152291.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr14:57752966 A>G maps to ENST00000431972 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr23:105450658 A>T did not map to a codon.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr23:105451020 C>G did not map to a codon.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr11:65632779 C>G maps to NM_025128.4 Y497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr6:49427026 C>A maps to NM_000255.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr16:88722099 G>A maps to NM_002461.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr12:110013870 G>A maps to NM_001114185.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr21:42767535 A>T maps to NM_002463.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr21:42749906 C>T maps to NM_002463.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr2:70142503 G>A maps to NM_002357.2 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr23:3241453 C>T did not map to a codon.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr23:3248742 T>G did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr23:3242750 C>A did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr23:3241096 G>C did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr23:3241267 G>A did not map to a codon.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr23:3235590 G>A did not map to a codon.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr17:4443018 C>T maps to NM_001105538.1 G1226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr12:102043145 T>C maps to NM_002465.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr1:109839552 C>T maps to NM_001010985.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr8:128751155 C>T maps to NM_002467.4 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr13:77625228 A>G maps to NM_015057.4 F4608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr1:40363241 C>G maps to NM_001033082.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr12:81112213 T>G did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr12:81101734 C>T maps to NM_002469.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr17:10400652 T>C maps to NM_005963.3 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr17:10398387 C>A maps to NM_005963.3 E1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr17:10395822 G>A maps to NM_005963.3 A1910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr17:10415996 C>T did not map to a codon.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr16:15835614 A>T did not map to a codon.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr16:15850215 G>A maps to NM_001040114.1 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr17:10212730 G>A maps to NM_003802.2 D1663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr17:10263336 A>T maps to NM_003802.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr17:10250011 C>T maps to NM_003802.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr17:10219342 C>T did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr19:50804964 C>G maps to NM_001145809.1 A1839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr19:50813045 G>C maps to NM_001145809.1 *2037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr3:108195348 A>T maps to NM_014981.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr3:108205365 G>C maps to NM_014981.1 L313L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-13-1497-01A-01W-0549-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr17:10435045 G>A maps to NM_017534.5 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr17:10432683 C>A maps to NM_017534.5 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr17:10432949 C>T maps to NM_017534.5 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr17:10541559 T>G maps to NM_002470.2 R1177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr17:10351710 A>T did not map to a codon.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr17:10366909 G>A maps to NM_017533.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr17:10351286 G>A maps to NM_017533.2 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr17:10356503 T>A maps to NM_017533.2 K1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr17:10350416 T>A maps to NM_017533.2 A1694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr14:23856749 C>G maps to NM_002471.3 L1546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr14:23900814 C>T maps to NM_000257.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1350-01A-01W-0490-10 chr20:33568864 T>G did not map to a codon.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr17:10304045 T>A maps to NM_002472.2 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr17:10309461 C>G maps to NM_002472.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr22:36698622 G>A maps to NM_002473.4 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr22:36696210 G>A maps to NM_002473.4 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr2:211158972 G>T maps to NM_079420.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr12:111356988 C>T maps to NM_000432.3 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr12:56553368 A>G did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr3:123441086 G>A maps to NM_053025.3 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr3:123451759 C>T maps to NM_053025.3 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr20:30419860 G>A maps to NM_033118.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr20:30419939 G>A did not map to a codon.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr16:46746654 G>A maps to NM_182493.2 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr17:18023082 G>A maps to ENST00000205890 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr17:18063310 A>C maps to ENST00000205890 T3122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr13:109777499 A>G maps to NM_015011.1 R1170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr13:109318423 G>A maps to NM_015011.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr13:109475515 C>T maps to NM_015011.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr17:34883525 C>A maps to NM_001163735.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr12:57431358 T>A maps to NM_005379.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1558-01A-01W-0615-10 chr12:57430805 G>A maps to NM_005379.2 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr17:31065330 C>G maps to NM_015194.1 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr15:59470657 C>G maps to NM_004998.2 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr19:8616668 G>A maps to NM_012335.3 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr2:171248911 A>T maps to NM_138995.3 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr15:52606343 A>G maps to ENST00000358212 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr18:47489317 C>G did not map to a codon.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr15:52571811 G>A maps to NM_018728.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr11:76870559 C>G maps to NM_000260.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr11:17741442 G>T maps to NM_002478.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr11:17742510 C>A maps to NM_002478.4 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr10:95123804 G>A maps to NM_013451.3 H927H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr8:2046691 C>T maps to NM_003970.2 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr8:2063846 T>A maps to NM_003970.2 I1092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr8:2057291 T>C maps to NM_003970.2 I1050I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1105-01A-01W-0484-10 chr1:24433675 G>A maps to ENST00000330966 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr10:75393677 G>T maps to NM_021245.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr10:75394422 G>C maps to NM_021245.2 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1659-01B-01W-0615-10 chr10:69955238 A>T maps to NM_032578.2 V1036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr3:40286040 G>A maps to NM_015460.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr3:40231702 C>T maps to NM_015460.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr10:76781769 C>T maps to NM_012330.2 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr20:62843482 G>A maps to NM_004535.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr2:1926913 G>A maps to ENST00000399161 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr2:1926807 G>T maps to ENST00000399161 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr2:1906915 A>G maps to ENST00000399161 Y656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr19:59082381 C>T maps to NM_198055.1 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr4:40144435 T>A maps to NM_018177.3 A1643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr13:32977285 C>A maps to NM_052818.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr13:32978396 G>A maps to NM_001079691.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr23:153195523 G>T did not map to a codon.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr4:140280991 C>G maps to NM_057175.3 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr13:41905482 A>G maps to NM_024561.4 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr12:112516500 C>T maps to NM_024953.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr12:112509773 G>A maps to NM_024953.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0801-01A-01W-0370-10 chr11:71192418 G>A maps to NM_018161.4 W339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr4:164061529 G>A maps to NM_138386.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr23:92927560 A>T did not map to a codon.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr23:92927380 G>A did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr23:92927625 T>G did not map to a codon.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr8:144657402 G>C maps to ENST00000276844 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr15:60740276 A>G maps to NM_024611.4 N729N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr8:18257939 C>T maps to NM_000015.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr8:18257818 C>T maps to NM_000015.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr2:73928243 G>A maps to NM_016347.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr1:201777828 A>C did not map to a codon.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr11:20077503 G>T did not map to a codon.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr12:78516136 G>A maps to NM_014903.4 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr2:15416993 C>T maps to NM_015909.2 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr2:15564501 C>G maps to NM_015909.2 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr2:15601356 T>G maps to NM_015909.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr13:35685047 C>T maps to ENST00000400445 H645H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr13:35770277 T>C maps to ENST00000400445 I1735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr2:204075811 T>G maps to NM_001114132.1 S2610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr1:19981645 C>T maps to NM_182744.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:19981858 C>T maps to NM_182744.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr1:19983390 G>C maps to NM_182744.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr8:90994997 G>A maps to NM_002485.4 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr1:16907928 T>C maps to NM_017940.3 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr1:16902855 C>T maps to NM_017940.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr1:148582429 C>T maps to NM_001170755.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr11:113133634 T>C maps to ENST00000397960 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr21:22656720 G>A did not map to a codon.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr21:22656619 C>T maps to NM_004540.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr12:6635332 C>T maps to NM_014865.3 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr11:134027821 C>A did not map to a codon.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr11:134046209 G>A maps to NM_015261.2 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr7:158476048 G>A maps to NM_017760.5 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr22:50960777 G>T maps to NM_001185011.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr19:39691102 A>T maps to NM_001001414.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr2:106471602 G>T maps to NM_001004720.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:183795489 T>C maps to NM_205842.1 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr12:54894408 G>T maps to NM_005337.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:133541587 A>T maps to NM_207363.2 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr2:232320316 G>A maps to NM_005381.2 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr2:232325560 A>T maps to NM_005381.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr2:24933861 G>A maps to NM_003743.4 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr20:46265283 C>T maps to NM_181659.2 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr6:126236496 A>C maps to NM_181782.4 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr12:124904571 G>T maps to NM_006312.4 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr12:124885182 G>A maps to NM_006312.4 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr18:2608739 G>A maps to NM_006101.2 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr16:15771671 G>A maps to NM_001143979.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr15:23932142 C>T maps to NM_002487.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr8:134269064 G>A maps to NM_006096.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr16:58538307 C>T maps to NM_001130487.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr2:240954194 G>A maps to ENST00000404554 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr18:9122596 G>A maps to NM_021074.4 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr21:44329128 T>G maps to NM_021075.3 *474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr2:152500387 G>A maps to NM_001164507.1 L2634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr2:152409233 A>G maps to NM_001164507.1 D6596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr2:152499123 G>T maps to NM_001164507.1 I2779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:152553149 C>T did not map to a codon.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr10:21101809 G>A maps to ENST00000430741 D804D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr10:21185901 C>T maps to ENST00000430741 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr10:21461355 G>A maps to NM_213569.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr16:84035456 G>A maps to NM_019065.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr16:84035481 C>T maps to NM_019065.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr12:8245637 A>G maps to NM_015509.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr18:55989691 T>C maps to NM_001144967.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr8:24771917 C>T maps to NM_005382.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr4:170345832 T>C maps to ENST00000507142 Q1031Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr3:27333073 A>G maps to ENST00000396636 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr3:130748708 C>T maps to NM_024800.4 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr1:156645081 G>T maps to NM_006617.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr1:156640106 G>A maps to NM_006617.1 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr18:70451072 C>A maps to NM_153181.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0911-01A-01W-0420-08 chr18:70526213 C>A maps to NM_153181.2 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr16:47117251 T>C maps to NM_018092.3 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr11:74705647 C>T maps to NM_006656.5 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr2:182543472 T>A maps to NM_002500.2 K39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr12:55420442 A>T maps to NM_021191.2 K74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr12:55420537 C>T maps to NM_021191.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr1:78383898 G>T maps to NM_144573.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr17:29490248 C>T maps to NM_001042492.2 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr17:29592268 G>T maps to NM_001042492.2 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr17:29509524 G>T did not map to a codon.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr17:29654604 C>A maps to NM_001042492.2 S1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr17:29670025 G>T did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr17:29665109 C>T maps to NM_001042492.2 R2258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr17:29664597 G>T maps to NM_001042492.2 E2214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr17:29576133 C>A maps to NM_001042492.2 Y1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr22:30090739 G>C did not map to a codon.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr22:30061030 C>G maps to NM_181832.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0801-01A-01W-0370-10 chr1:204923323 G>A maps to ENST00000367172 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr18:77227619 G>A maps to NM_172390.1 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr20:50140458 C>T maps to NM_012340.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr17:46136558 C>T maps to ENST00000362042 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr7:26224973 T>C maps to NM_004289.6 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr4:103459064 A>G maps to NM_003998.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr3:101574575 G>T did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr11:129739826 G>A maps to NM_006165.3 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr20:34268745 G>A maps to NM_021100.4 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr20:34262981 T>G maps to NM_021100.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr2:233791838 G>A maps to NM_019850.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr17:47583823 G>A maps to NM_002507.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr4:103867938 T>C maps to NM_139173.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr6:18121871 G>T maps to NM_198586.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr6:18122525 A>G maps to NM_198586.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr6:18122525 A>G maps to NM_198586.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr10:115657950 C>G maps to NM_198514.3 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr23:17743956 T>G did not map to a codon.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr23:17750348 C>T did not map to a codon.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr3:49463699 C>T maps to NM_032316.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr3:49463717 T>A maps to NM_032316.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr14:52534881 C>G did not map to a codon.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr12:675224 C>T maps to NM_016533.4 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr20:25459746 C>T maps to NM_025176.4 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr20:25484689 C>A maps to NM_025176.4 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr5:36985863 C>A maps to NM_133433.3 S861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr5:37000974 A>T maps to NM_133433.3 K1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr22:29954896 C>T maps to NM_003634.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr3:52526017 C>G maps to NM_007184.3 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr1:31654705 C>G did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:119077311 G>A did not map to a codon.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:119077252 G>A did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr23:118723740 G>A did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:118723533 G>T did not map to a codon.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:118724127 T>A did not map to a codon.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr20:21376926 C>A maps to NM_033176.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr23:70387452 C>G did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:70387253 T>C did not map to a codon.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr23:5821715 T>C did not map to a codon.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr23:6069175 G>A did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr16:3598754 T>C did not map to a codon.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr2:32475575 G>A maps to NM_021209.4 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr16:57089398 G>A maps to NM_032206.3 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr17:5462707 C>T maps to NM_033004.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr11:7982396 C>T maps to NM_176821.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr19:56307534 C>G maps to NM_145007.3 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr19:56307616 C>A did not map to a codon.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr19:56320355 C>T maps to NM_145007.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr19:54313397 G>A maps to ENST00000391773 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr19:54312881 G>A maps to ENST00000391773 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr19:56423112 A>G maps to NM_176810.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr19:56423124 C>T maps to NM_176810.2 K686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr19:56423808 A>G maps to NM_176810.2 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr11:7079615 T>A maps to NM_176822.3 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr11:7071012 A>T maps to NM_176822.3 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr19:55501459 C>T maps to NM_017852.3 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr1:247599442 G>C did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr1:247587803 G>A maps to NM_004895.4 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr19:56565057 C>T maps to NM_153447.4 I1061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr19:55450535 G>A maps to ENST00000446217 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr19:56466122 C>T maps to NM_176811.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr19:56477746 G>T did not map to a codon.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr19:56466194 C>T maps to NM_176811.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr19:56241219 A>T maps to NM_176820.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr19:56249719 C>T maps to NM_176820.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr3:160952913 T>A maps to ENST00000472947 L164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr16:449123 G>A did not map to a codon.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr2:232393124 G>T maps to NM_006056.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr5:151783972 G>A maps to NM_020167.4 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr5:43659362 G>T maps to NM_182977.2 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr5:43656872 C>T maps to NM_182977.2 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr5:43613217 G>T maps to NM_182977.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr16:50745532 C>T maps to NM_022162.1 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr17:65734279 G>A maps to NM_015462.3 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr18:31523136 T>C maps to NM_003787.4 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr9:33466930 T>C maps to NM_022917.4 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr9:33466614 C>T maps to NM_022917.4 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr1:6589099 C>A maps to NM_024654.4 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr7:156759097 T>A did not map to a codon.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr16:14980652 A>C maps to ENST00000456867 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:70511752 A>C did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr23:70514364 T>C did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:70519851 G>T did not map to a codon.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr12:6675290 A>C maps to ENST00000382421 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr12:6666621 G>T maps to ENST00000382421 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr20:2636147 G>A maps to NM_006392.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr17:26101405 G>C maps to NM_000625.4 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr1:120491094 T>C maps to NM_024408.2 E898E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr19:15298003 G>A maps to NM_000435.2 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr19:15281227 G>A maps to NM_000435.2 F1676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr19:15281295 G>A maps to NM_000435.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr6:32188308 C>G maps to NM_004557.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr6:32180910 C>T did not map to a codon.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr6:32180353 G>T maps to NM_004557.3 C859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr19:46443348 C>T maps to NM_002516.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr23:100117758 G>T did not map to a codon.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr19:47542390 C>G maps to NM_002517.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr2:101604707 G>A maps to NM_002518.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr2:101580580 A>G maps to NM_002518.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr11:108032260 T>C maps to NM_002519.2 S1184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr8:53853429 G>A maps to NM_005285.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr18:21121350 C>A maps to NM_000271.4 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr18:21121118 G>A maps to NM_000271.4 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr18:21114409 G>A maps to NM_000271.4 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr7:44556454 G>A maps to NM_013389.2 P1149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr7:44579341 G>T maps to NM_013389.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1575-01A-01W-0615-10 chr7:44560364 T>C maps to NM_013389.2 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr17:45664703 T>G maps to NM_006310.3 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr4:72994448 C>A maps to NM_004885.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr19:36333451 C>A maps to NM_004646.3 G779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr19:36321760 G>A maps to NM_004646.3 Y1193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr19:36322248 G>A maps to NM_004646.3 N1112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr1:179528828 C>T maps to NM_014625.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr1:182787733 G>A maps to NM_030769.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr4:106863580 G>A maps to ENST00000503451 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr1:11918480 C>A maps to NM_002521.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:153659677 C>A maps to NM_000906.3 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr1:153659764 G>A maps to NM_000906.3 K675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr9:35805825 G>C did not map to a codon.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr16:150410 C>T maps to ENST00000399953 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr7:34867175 G>C maps to NM_207172.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr7:34698123 G>T maps to NM_207172.1 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr4:164272348 C>T maps to NM_006174.2 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr6:3015828 G>A maps to NM_000904.3 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr23:30326340 G>A did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr17:38256335 C>T maps to NM_021724.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1623-01A-01W-0615-10 chr12:100930825 G>A did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:161199715 C>A maps to NM_001077482.1 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr12:95445551 G>A maps to NM_003297.2 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr12:95445632 T>C maps to NM_003297.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr5:92929389 C>T maps to NM_005654.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr4:149035326 C>T maps to ENST00000511528 K913K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr2:157183360 C>A maps to NM_006186.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr2:157186266 G>A maps to NM_006186.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr9:127262731 C>T maps to NM_004959.4 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:200017450 T>C maps to NM_205860.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr9:127298391 C>A maps to NM_033334.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr10:115423590 C>T maps to ENST00000369358 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr1:115258685 A>C maps to NM_002524.3 Y32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr7:107818498 C>T maps to ENST00000379032 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr7:107825023 C>T maps to ENST00000379032 K690K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr7:107834871 C>T maps to ENST00000379032 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr8:32472041 T>G maps to NM_013956.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr23:105132357 C>T did not map to a codon.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr23:105156664 A>G did not map to a codon.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr23:105153287 A>T did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:206641108 C>T maps to NM_018534.3 H860H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr2:206592643 G>A maps to NM_201266.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr6:24145906 G>A maps to NM_080723.4 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr2:50850721 T>A maps to ENST00000404971 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr2:50318608 C>T maps to ENST00000404971 K1230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr2:50758413 G>T maps to ENST00000404971 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr11:64390410 G>T maps to NM_015080.3 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr11:64418974 C>T maps to NM_015080.3 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr11:64453369 G>A maps to NM_015080.3 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr14:79746759 C>T maps to ENST00000440563 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr5:74066517 T>C maps to NM_014886.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr5:176715817 A>C did not map to a codon.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr17:44828912 G>A maps to NM_006178.2 Q696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr10:18940059 C>A maps to NM_182543.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr6:86200328 C>T maps to NM_002526.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr11:132184607 G>T maps to NM_001144059.1 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr11:132016193 G>A maps to NM_001144058.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr1:107867514 C>G maps to NM_001113226.1 Y286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr1:156846211 G>A maps to NM_002529.3 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:156849009 C>T maps to NM_002529.3 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr1:156837922 T>C maps to NM_002529.3 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr1:156845441 A>G maps to NM_002529.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr9:87342779 C>T maps to NM_006180.3 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr15:88576169 C>G maps to NM_001012338.1 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr15:88483903 C>A maps to NM_001012338.1 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr15:88522596 G>A maps to NM_001007156.1 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr12:106460897 G>C maps to NM_014840.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr1:205273312 G>A maps to ENST00000441520 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr1:205273342 G>C maps to ENST00000441520 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr1:205277291 C>T did not map to a codon.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:51239267 G>T did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:51239215 G>A did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr3:131102091 C>T maps to NM_152395.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr1:145587452 G>A maps to NM_001012758.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr16:77759481 G>T did not map to a codon.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr1:163317603 T>C maps to NM_145697.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr11:71725593 C>A maps to ENST00000393695 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:229622189 C>T maps to NM_018230.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr5:37318110 C>A maps to NM_153485.1 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr5:37299661 C>T maps to NM_153485.1 G1190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr5:37307523 A>C maps to NM_153485.1 Y926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr5:37327816 G>A maps to NM_153485.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr5:37330174 T>C maps to NM_153485.1 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr11:47869813 G>A maps to NM_015231.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr11:47814441 G>T maps to NM_015231.1 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr9:131745577 G>A maps to NM_015354.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr7:135287640 A>G maps to NM_015135.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr3:13378307 G>A maps to NM_024923.2 D1221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr3:13359230 T>A maps to NM_024923.2 K1872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr3:13407547 T>G maps to NM_024923.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr1:154098924 T>C maps to NM_207308.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr9:134108872 G>A maps to ENST00000451030 *2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr9:134003074 A>G maps to ENST00000451030 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr19:16870239 G>A did not map to a codon.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr23:101615532 G>T did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr23:101624568 G>A did not map to a codon.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr23:101572403 C>T did not map to a codon.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr23:102339342 T>C did not map to a codon.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr23:102338569 C>G did not map to a codon.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr17:704245 G>A maps to NM_022463.3 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr2:139429226 A>T maps to NM_007226.2 C20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr2:139428868 C>A maps to NM_007226.2 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1525-01A-01W-0615-10 chr23:108780234 G>T did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr23:108779197 C>A did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr23:41334056 G>T did not map to a codon.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr12:113442914 C>G maps to NM_016817.2 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr12:121458605 G>A maps to NM_003733.2 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr12:121469367 G>A maps to NM_003733.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr10:105658747 G>A maps to NM_024928.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr12:56620150 C>T maps to NM_024068.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr1:228482622 C>G maps to NM_001098623.1 Y3846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr1:228479626 G>A maps to NM_001098623.1 L3456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr2:220432566 C>T maps to NM_015311.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr8:133045303 C>A maps to ENST00000262283 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr8:133036961 G>T maps to ENST00000262283 C612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr8:133051070 G>T maps to ENST00000262283 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr15:28260040 G>A maps to NM_000275.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr23:128724234 C>T did not map to a codon.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr23:128724127 C>T did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr9:131256967 G>T maps to ENST00000372814 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr11:197576 G>A maps to NM_053280.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr23:123517889 C>A did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr23:123517986 G>A did not map to a codon.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr23:123787618 G>A did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr23:123631095 A>T did not map to a codon.
Sequencing variant TCGA-24-0966-01A-01W-0977-09 chr23:123518181 G>C did not map to a codon.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr23:123517632 C>T did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:123775706 T>A did not map to a codon.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr23:123785912 T>C did not map to a codon.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr23:123517987 C>T did not map to a codon.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr23:124029955 C>G did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr23:123517674 C>G did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr23:124097585 C>T did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:123518242 T>A did not map to a codon.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr23:123787437 G>T did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr23:123518148 C>G did not map to a codon.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr5:167517658 C>A maps to NM_001122679.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr10:50952142 G>C maps to NM_018245.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr9:95155464 G>A maps to NM_033014.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr23:70776598 G>T did not map to a codon.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:70757808 C>T did not map to a codon.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr23:70777084 C>A did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr9:137987846 C>T maps to NM_014279.4 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:102462357 G>C maps to NM_058170.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr13:53624716 C>A maps to NM_006418.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr11:7509632 T>A maps to NM_198474.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr11:7531331 C>T maps to NM_198474.3 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr11:132307167 C>T maps to NM_002545.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr11:132399048 G>A maps to NM_002545.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr23:67454405 C>G did not map to a codon.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr23:67283808 G>T did not map to a codon.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr23:153418459 C>A did not map to a codon.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr23:153421875 C>A did not map to a codon.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr23:153418473 G>C did not map to a codon.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr6:47763299 G>C did not map to a codon.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr8:54142198 G>A maps to NM_000912.3 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr6:154411137 C>T maps to NM_001145279.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr11:7961025 G>A maps to NM_001003745.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr12:55615677 C>T maps to NM_001005280.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr11:55735357 C>T maps to NM_001005491.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr11:123909522 G>T maps to NM_001004463.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr11:123901210 G>T maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr11:123893853 G>A maps to NM_001001953.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr19:15918748 C>A maps to NM_013940.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr19:15917977 G>A maps to NM_013940.2 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr19:15839077 G>A maps to NM_013939.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr19:15839641 C>A maps to NM_013939.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr19:16060302 G>A maps to NM_001004465.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr1:159283702 G>A maps to NM_001004467.1 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr1:159505233 G>A maps to NM_001004469.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr12:56031517 C>A maps to NM_206899.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr11:57995921 G>A maps to NM_001004471.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr11:57995624 C>T maps to NM_001004471.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr11:58034595 G>T maps to NM_207374.3 C245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr1:158549275 G>T maps to NM_001004477.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr14:19377699 G>A maps to NM_001013354.1 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr14:20711204 C>T maps to NM_001004479.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr6:29365184 C>T maps to NM_013936.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr9:107332185 A>C maps to NM_001004483.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr9:107457622 G>A maps to NM_001004484.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:130678869 G>A did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr1:248844846 C>A maps to NM_001004734.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr1:248845155 G>T maps to NM_001004734.1 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2409-01A-01W-0799-08 chr9:125424242 G>A maps to ENST00000373686 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr9:125512887 G>A maps to ENST00000373684 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr9:125377714 C>T maps to NM_012364.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr11:57971086 G>A maps to NM_001004459.1 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr7:143747796 C>A maps to NM_012365.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr7:143748036 C>T maps to NM_012365.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr7:143748084 G>A maps to NM_012365.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr1:247614819 A>G maps to NM_001004492.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr1:247614504 A>T maps to NM_001004492.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr6:27925341 G>T maps to NM_012367.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr16:3406248 C>T maps to NM_012368.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1666-01A-01W-0615-10 chr11:6913263 A>C maps to NM_003700.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr7:143657359 C>T maps to NM_012369.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr1:248685714 A>T maps to NM_001013355.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr6:29141852 G>A maps to NM_030905.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr9:114090590 G>T maps to ENST00000374428 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr1:248402272 C>T maps to NM_017504.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1116-01A-01W-0486-08 chr1:248308538 G>T maps to NM_001004690.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr1:248458841 T>C maps to NM_001004692.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr1:248616850 T>G maps to NM_001004136.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr1:248616271 A>C maps to NM_001004136.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr1:248551172 C>T maps to NM_001005471.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr1:247654758 C>A maps to NM_001004698.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr5:180166788 G>C maps to NM_001001657.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr5:180166170 C>A maps to NM_001001657.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr19:8841587 C>G maps to NM_001004699.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr19:8841879 C>T maps to NM_001004699.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr17:3181523 G>A maps to NM_002551.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr11:55110732 T>G maps to NM_001005274.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr11:51411930 C>T maps to NM_001005272.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr11:51411696 G>A maps to NM_001005272.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1603-01A-01W-0551-08 chr11:51411669 G>C maps to NM_001005272.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr11:55339858 A>T maps to NM_001004701.2 K86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr11:59245207 T>C maps to NM_001004705.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr11:59271584 C>T maps to NM_001004706.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr11:59282495 A>T maps to NM_001004711.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr14:22134198 C>G maps to NM_001001912.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr14:22133307 A>C maps to NM_001001912.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr14:20502053 T>C maps to NM_001004714.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr14:20483061 T>C maps to NM_001004712.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0891-01A-01W-0420-08 chr14:20389055 C>T maps to NM_001005483.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1586-01A-02W-0633-09 chr14:20528940 G>T maps to NM_001004717.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr15:22382869 C>A maps to NM_001005241.1 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr15:22382564 C>A maps to NM_001005241.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr15:22382522 G>C maps to NM_001005241.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr14:20612415 C>T maps to NM_001004724.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr11:55406021 C>G maps to NM_001004124.1 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr11:55418513 G>T maps to NM_001004059.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr11:5345005 A>C maps to NM_033180.4 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr11:5364097 T>A maps to NM_001005567.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr11:4870048 C>G maps to NM_001004758.1 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr11:4903875 A>C maps to NM_001004759.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr11:5172993 A>G maps to NM_012375.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr11:5141962 G>C maps to NM_001005222.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr11:5152971 G>A maps to NM_001005160.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr11:5079963 C>T maps to NM_001005164.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr11:5080593 C>T maps to NM_001005164.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr11:5906139 T>C maps to NM_001005165.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr11:5878215 T>A maps to NM_001005168.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr11:5566537 G>C maps to NM_001005289.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr11:4608092 C>T maps to NM_001005170.2 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr11:4471462 C>T maps to NM_001005172.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr11:5810025 G>A maps to NM_001001913.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr11:6023856 G>C maps to NM_001005179.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr11:59211349 C>T maps to NM_001004728.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr11:59211066 C>T maps to NM_001004728.1 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr11:56757316 A>C maps to NM_001005323.1 *310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1471-01A-01W-0551-08 chr11:56756786 T>C maps to NM_001005323.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr11:56756894 C>A maps to NM_001005323.1 C169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr11:59132146 C>G maps to NM_001004729.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr11:55798730 T>G maps to NM_001001921.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr11:55798442 T>C maps to NM_001001921.1 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr11:58190044 C>T maps to NM_001005566.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr11:58190662 G>T maps to NM_001005566.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr11:58275167 A>G maps to NM_001005218.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr11:55563432 T>C maps to NM_001004735.1 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr11:55563156 A>G maps to NM_001004735.1 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr11:55606373 G>A maps to NM_001005496.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr11:55761771 G>A maps to NM_003697.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr11:55703699 G>A maps to NM_006637.1 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr11:55944593 C>G maps to NM_001005492.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr3:98216961 A>T maps to NM_001004737.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr3:98110426 A>G maps to NM_001005516.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr3:98073008 C>A maps to NM_001005517.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr11:55579055 G>A maps to NM_001004738.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr11:56380659 G>A maps to NM_001004740.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr11:56380396 G>C maps to NM_001004740.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr11:56237478 G>A maps to NM_001004742.1 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr11:56230433 G>C maps to NM_001004743.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr11:56044079 C>T maps to NM_001004745.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr11:56000394 A>G maps to NM_001004746.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr6:29323462 G>A maps to NM_030876.5 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr7:143701919 C>T maps to NM_001005281.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr12:55714820 T>G maps to NM_001005182.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr12:55846842 G>A maps to NM_054105.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr1:158724892 C>T maps to NM_001005184.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:158736358 A>G maps to NM_001005185.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr14:21109628 C>T maps to NM_001001968.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr11:123624728 G>A maps to NM_001005188.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr11:123624989 C>T maps to NM_001005188.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr19:14952575 A>T maps to NM_001005190.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr19:14991669 C>G maps to NM_030901.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr19:15052698 G>A maps to NM_012377.1 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr19:15052653 G>A maps to NM_012377.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr19:9297068 T>A maps to NM_175883.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr19:9325423 C>G maps to NM_001005191.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr19:9324679 G>A maps to NM_001005191.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr19:9225596 G>T maps to ENST00000293614 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr19:9236798 C>A maps to NM_001001958.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr11:124440467 C>A maps to NM_001005194.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr11:124253128 G>T maps to NM_001005468.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr11:124095489 A>G maps to NM_001007249.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr11:124135294 G>A maps to NM_001005198.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr11:56057992 T>G maps to NM_001005199.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr11:56057869 G>T maps to NM_001005199.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr11:55890078 C>A maps to NM_001005201.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr11:55890363 C>T maps to NM_001005201.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr11:55861622 C>T maps to NM_001003750.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr11:55904978 G>A maps to NM_001004064.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr11:56085841 C>A maps to NM_001005202.1 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr11:56086255 A>T maps to NM_001005202.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr11:55927094 G>T maps to NM_001004058.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr11:55927007 G>T maps to NM_001004058.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr11:56510657 G>A maps to NM_001005284.1 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr11:57947149 C>T maps to NM_001005212.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr2:201790655 C>A did not map to a codon.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr2:148693162 A>G maps to NM_181742.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr7:103801603 T>C maps to NM_002553.3 K355K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr9:117092748 T>C maps to NM_000608.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr12:58113915 C>A maps to NM_006812.3 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr18:21746585 G>A maps to NM_080597.2 C872C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr3:195959312 A>C maps to NM_152672.5 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr3:195955760 C>T maps to NM_152672.5 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:38211975 A>T did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr2:26697479 C>T maps to NM_194248.2 A1063A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr2:26712160 C>A maps to NM_194248.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr2:26698895 C>T maps to NM_194248.2 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr4:4199525 C>T maps to NM_177998.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr14:94511023 G>T maps to NM_023112.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr8:92082605 G>T maps to NM_016023.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr2:63282934 G>C maps to NM_014562.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr12:29630328 T>C maps to NM_183378.2 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr3:25833482 C>G maps to NM_017897.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr17:3807286 G>A maps to NM_002558.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr12:121622367 C>G maps to NM_002562.5 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr3:152553924 C>A maps to NM_002563.2 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr23:78216069 C>G did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:78216713 C>A did not map to a codon.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr10:74810981 A>T maps to NM_000917.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr11:74009310 C>T maps to NM_182904.3 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr23:90691012 G>C did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:90691048 C>A did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr11:65983654 T>C maps to NM_018026.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr11:66000525 G>C maps to NM_018026.2 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr1:17555196 G>T maps to NM_013358.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr1:17410238 T>A maps to NM_007365.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr1:17685854 C>T maps to NM_012387.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr1:17664576 G>A maps to NM_012387.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr23:55117790 G>T did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:55117042 G>T did not map to a codon.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr12:103237491 G>A maps to NM_000277.1 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr12:103246707 G>A maps to NM_000277.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr12:103249097 G>A maps to NM_000277.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr11:77047307 T>G maps to NM_001128620.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr11:77066711 C>A did not map to a codon.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:110437552 G>T did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr23:110388129 A>T did not map to a codon.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr23:110366476 G>T did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr23:110459765 T>C did not map to a codon.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr23:110366349 A>G did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr19:39669140 G>A maps to NM_005884.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr15:40568132 C>T maps to NM_020168.4 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr20:9561001 G>A maps to NM_177990.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr16:23646758 G>A maps to NM_024675.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr4:169824954 C>T maps to NM_001166108.1 H840H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr19:746345 G>A maps to NM_002579.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr11:35457457 G>T maps to NM_015430.2 C459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr12:56718840 A>C maps to NM_001127460.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr14:97022189 C>T maps to NM_032632.3 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr7:4901291 G>A maps to NM_020144.4 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr9:119093632 C>A maps to NM_002581.3 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr1:176740241 C>T maps to NM_020318.2 D1547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr1:176661370 C>T maps to NM_020318.2 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr4:79860318 C>T maps to NM_001040202.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr15:69677129 C>T maps to NM_017705.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr1:156214681 C>T maps to NM_024897.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr10:34671759 T>C maps to NM_019619.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr10:51087744 A>G maps to NM_003631.2 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr1:226566919 G>A maps to NM_001618.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr7:139724413 C>G maps to NM_022750.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr7:139727146 G>A maps to NM_022750.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr7:139746808 T>A did not map to a codon.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr3:122437032 G>T maps to NM_017554.2 L1372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr3:122422731 A>T maps to NM_017554.2 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr15:65559013 G>A maps to NM_017851.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr5:50128648 C>T maps to ENST00000505697 D756D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr3:122277230 G>T maps to NM_031458.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr1:55223916 C>T maps to NM_152268.3 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr1:55223579 C>A maps to NM_152268.3 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:150842516 A>T did not map to a codon.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr23:150793953 C>T did not map to a codon.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr23:150842506 C>T did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:150840810 C>A did not map to a codon.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr2:242076502 G>C maps to ENST00000358649 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1574-01A-01W-0615-10 chr2:242046884 G>A maps to ENST00000358649 Q1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr11:59423057 G>C maps to NM_152716.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:127253097 G>C maps to NM_006193.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr11:31815585 T>C maps to NM_001604.4 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr2:113999126 C>A did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr7:154760665 C>T maps to NM_007349.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr10:70048419 T>G did not map to a codon.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr3:52692280 T>G maps to ENST00000296302 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr3:52623161 G>C maps to ENST00000296302 Y963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr11:66618549 T>C maps to NM_022172.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr11:66639504 C>G maps to NM_022172.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr12:53861066 C>T maps to NM_005016.5 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr5:141248322 C>T maps to NM_032420.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr5:141243375 C>G maps to NM_032420.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr23:91132871 A>T did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr5:141331059 G>A maps to NM_016580.2 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0975-01B-02W-0486-08 chr5:141337203 C>G maps to NM_016580.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr10:55849748 T>A maps to NM_001142763.1 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr10:55755491 G>A maps to NM_001142763.1 R934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr10:55955462 G>A maps to NM_001142763.1 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr10:55571357 T>C maps to ENST00000395438 E1465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr10:55955526 A>G maps to NM_001142763.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr10:55568457 T>A maps to NM_001142769.1 A1789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr10:55944983 T>A maps to NM_001142763.1 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr13:58208326 G>A maps to NM_001040429.2 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr23:99662582 T>A did not map to a codon.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr23:99551802 G>A did not map to a codon.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr23:99551782 C>T did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:99661899 G>A did not map to a codon.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr23:99551360 C>A did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr13:61986436 G>T maps to NM_022843.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr4:30726070 C>T maps to NM_001173523.1 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr13:67205408 G>A maps to NM_203487.2 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr13:67800286 C>T maps to NM_203487.2 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr5:140167317 C>T maps to NM_018900.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr5:140389305 C>T maps to NM_018909.2 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr5:140236991 G>A maps to NM_018901.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2038-01A-01W-0722-08 chr5:140257111 C>T maps to NM_018903.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr5:140262566 C>T maps to NM_018904.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr5:140263295 C>T maps to NM_018904.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr5:140175781 C>T maps to NM_018905.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr5:140174980 A>G maps to NM_018905.2 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr5:140182137 G>A maps to NM_018906.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr5:140182395 C>T maps to NM_018906.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr5:140181288 T>G maps to NM_018906.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr5:140182629 C>T maps to NM_018906.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr5:140188832 G>C maps to NM_018907.2 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr5:140186855 C>T maps to NM_018907.2 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr5:140188136 C>T maps to NM_018907.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr5:140202550 G>A maps to NM_018908.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr5:140202913 G>A maps to NM_018908.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr5:140215374 G>A maps to NM_018910.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr5:140229993 C>T maps to NM_031857.1 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr5:140306533 G>A maps to NM_018898.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr5:140306755 C>T maps to NM_018898.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr5:140308285 G>A maps to NM_018898.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr5:140347637 A>G maps to NM_018899.5 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr5:140432710 C>G maps to NM_013340.2 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr5:140574498 C>T maps to NM_018930.3 R792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr5:140590509 C>T maps to NM_018932.3 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr5:140595572 C>T maps to NM_018933.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr5:140603478 A>C maps to NM_018934.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr5:140604912 C>T maps to NM_018934.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr5:140626303 G>A maps to NM_018935.2 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr5:140562640 C>T maps to NM_020957.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr5:140474406 G>T maps to NM_018936.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr5:140482497 G>A maps to NM_018937.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr5:140502020 G>A maps to NM_018938.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr5:140554152 G>A maps to NM_018940.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr5:140559366 C>G maps to NM_019120.2 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr5:140567926 T>G maps to NM_019119.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr5:140712161 G>A maps to NM_018912.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr5:140794664 G>T maps to NM_018913.2 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr5:140794529 G>T maps to NM_018913.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr5:140802530 G>A maps to NM_018914.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr5:140801597 G>A maps to NM_018914.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr5:140746309 C>T maps to NM_018918.2 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr5:140745300 T>G maps to NM_018918.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr5:140774125 A>G maps to NM_032088.1 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr5:140740781 G>A maps to NM_018923.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr5:140768890 G>T maps to NM_003736.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr5:140789112 C>T maps to NM_018926.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1546-01A-01W-0615-10 chr5:140866164 C>A maps to NM_018928.2 C475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr11:82868480 A>C did not map to a codon.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr20:44574846 C>T maps to NM_022104.3 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr20:56139414 G>A maps to NM_002591.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr20:56136664 C>T maps to NM_002591.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr20:56138628 T>A maps to NM_002591.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr7:82764556 G>T maps to NM_033026.5 S770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr7:82784252 C>T maps to NM_033026.5 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr7:82585726 T>C maps to NM_033026.5 E1514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr7:82538329 C>A did not map to a codon.
Sequencing variant TCGA-25-2409-01A-01W-0799-08 chr8:17872111 T>C maps to NM_006197.3 P1868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr6:150092349 C>T maps to NM_005389.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr21:47851838 C>T maps to NM_006031.5 Q2821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr3:142542455 A>G maps to NM_013363.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr5:95728745 G>A maps to NM_000439.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr9:78710933 C>T maps to NM_001190482.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr10:112641174 G>T maps to NM_014456.4 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr3:33894095 A>T maps to NM_001162429.1 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr6:165752847 C>A did not map to a codon.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr6:165829726 T>C maps to NM_001130690.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr2:178762865 G>T maps to NM_016953.3 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr2:178684974 A>G maps to NM_016953.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr3:57542915 A>C maps to NM_177966.5 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr7:31918637 G>A maps to NM_001191057.1 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr11:72296637 C>A did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr12:20769279 C>T maps to NM_000921.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr19:10571777 C>A maps to NM_001111307.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr1:66829220 G>T maps to NM_001037341.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr19:18321933 G>A maps to NM_000923.3 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr1:144879282 C>A maps to NM_014644.4 S1389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr1:144952199 C>T maps to NM_022359.5 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr5:149324229 C>A maps to NM_000440.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr10:95380444 G>T maps to NM_006204.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr12:15131080 G>C did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr15:85610363 G>A maps to NM_002605.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr5:76621404 C>A maps to NM_003719.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr5:76624858 G>C maps to NM_003719.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr4:55155050 C>T maps to ENST00000507166 H680H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr4:55144646 C>A maps to ENST00000507166 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr23:19367443 G>A did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr4:96762458 C>T maps to NM_005390.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr3:58414284 G>A maps to NM_000925.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr7:148702413 C>T maps to NM_004911.4 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr3:122880169 T>A maps to NM_006810.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr3:122829810 G>A maps to NM_006810.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr16:20371967 A>T maps to NM_174924.1 Y476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr2:173460654 C>T maps to ENST00000392571 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:24546200 C>A did not map to a codon.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr23:24523396 G>A did not map to a codon.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr4:186427685 G>A maps to NM_014476.4 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr5:131607825 G>A maps to NM_003687.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr16:66919155 G>A maps to NM_020786.2 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr6:107595358 T>C maps to NM_020381.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr6:107595388 A>C maps to NM_020381.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr22:38061649 C>T maps to ENST00000442465 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr5:31983259 G>T did not map to a codon.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr5:32087828 G>A maps to NM_178140.2 T1425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr3:73433880 G>A maps to NM_015009.1 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr12:41946498 C>A maps to NM_001164595.1 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr1:156874644 G>A did not map to a codon.
Sequencing variant TCGA-13-0911-01A-01W-0420-08 chr19:57328816 T>C maps to NM_006210.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr19:57328939 T>C maps to NM_006210.2 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr11:66240743 C>T maps to NM_145065.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr19:33980957 G>A maps to NM_000285.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr17:8052944 G>A maps to NM_002616.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr17:8045155 C>G maps to NM_002616.2 R1189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr17:8047119 G>A maps to NM_002616.2 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr17:8049357 C>A maps to NM_002616.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr7:92147159 C>T maps to NM_000466.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr11:45937073 G>T maps to NM_057174.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr8:77896008 T>A maps to NM_001172087.1 K136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr22:18570810 T>G maps to NM_017929.5 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr12:7361750 C>T maps to NM_001131023.1 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr12:7361145 C>T maps to NM_001131023.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr3:179592211 C>G did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr17:8158833 G>A maps to NM_012393.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr12:53690059 G>C did not map to a codon.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr23:55020431 T>G did not map to a codon.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr23:54960255 C>G did not map to a codon.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr10:6261551 G>A maps to NM_004566.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0975-01B-02W-0486-08 chr12:48529114 C>G maps to NM_001166686.1 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr11:60971722 C>A maps to NM_001079807.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr11:60975041 C>T maps to NM_001079807.1 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr2:197781282 T>C maps to NM_024989.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0927-01A-02W-0419-10 chr6:28269964 C>T maps to NM_032507.3 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr6:28269715 C>T maps to NM_032507.3 I695I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr10:50724734 G>T maps to ENST00000515869 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr1:230513264 G>A maps to ENST00000321327 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr5:114552670 C>G did not map to a codon.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr23:77369243 T>G did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr19:46522496 C>T maps to NM_005091.2 *197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr19:15582816 C>A maps to NM_052890.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr1:153303305 T>C maps to NM_020393.2 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr1:64102038 C>T maps to NM_002633.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr11:74056675 G>A maps to NM_173582.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr11:74053597 T>A maps to NM_173582.3 K514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr9:71144547 G>A maps to NM_021965.3 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr20:58318323 G>A did not map to a codon.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr23:22115156 G>T did not map to a codon.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr23:22129651 C>G did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr6:33382136 G>A maps to NM_024165.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr9:96416840 C>T maps to NM_005392.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr8:133851827 G>A did not map to a codon.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr8:133807001 T>C maps to ENST00000395386 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2408-01A-01W-0799-08 chr6:64416111 A>T maps to NM_015153.2 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr23:133549044 G>C did not map to a codon.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr3:52456306 C>A maps to ENST00000454052 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr23:54069218 G>A did not map to a codon.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr23:54020322 T>C did not map to a codon.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr23:54026304 C>T did not map to a codon.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr23:54011431 C>G did not map to a codon.
Sequencing variant TCGA-29-2436-01A-01D-1526-09 chr23:53966649 G>A did not map to a codon.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr23:53989291 G>T did not map to a codon.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr1:120284483 G>A maps to NM_006623.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr6:79655098 T>C maps to NM_017934.5 E1582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr6:79650904 C>T maps to NM_017934.5 K1657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:71856223 C>G did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr23:71830999 G>A did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:71846833 A>T did not map to a codon.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr23:71864274 C>A did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr23:71813120 G>T did not map to a codon.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr16:47623000 A>G maps to NM_000293.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr16:30768417 G>A maps to NM_000294.2 *407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr3:111693367 T>C maps to NM_001134438.1 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr3:111604102 A>T maps to NM_001134438.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr19:43990787 C>T maps to NM_198850.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr8:75756232 T>A maps to NM_015886.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr8:75737572 C>A maps to NM_015886.3 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr4:25258232 G>A maps to NM_018323.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr15:68434290 C>T maps to NM_016166.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2088-01A-01W-0722-08 chr23:15349504 C>T did not map to a codon.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr2:46839389 C>T maps to NM_002643.3 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1576-01A-01W-0615-10 chr1:77627338 T>G maps to NM_005482.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr1:160000818 C>A maps to NM_145167.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr1:160000752 A>G maps to NM_145167.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr9:35092718 G>A maps to NM_032634.2 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr1:27121256 G>T maps to NM_017837.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr3:196678887 T>A maps to NM_025163.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr10:98383241 C>T maps to NM_152309.2 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr1:204403037 A>G maps to NM_002646.3 Y1242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr12:18658245 C>T maps to NM_004570.4 Y1017Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr12:18499746 C>T maps to NM_004570.4 N534N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr18:39600609 C>A maps to ENST00000398870 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr3:178928343 C>T maps to NM_006218.2 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr3:178942592 C>A maps to NM_006218.2 I800I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr3:178917652 A>G maps to NM_006218.2 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr7:106509370 G>A maps to NM_002649.2 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr22:31679150 C>G maps to NM_052880.4 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr5:67593404 A>C maps to ENST00000396611 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr5:67588085 G>C did not map to a codon.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr19:18273866 C>T maps to NM_005027.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr3:130425974 T>C maps to NM_014602.2 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr2:209218726 C>T maps to NM_015040.3 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr2:209200595 A>T maps to NM_015040.3 K1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr1:20971139 C>A maps to NM_032409.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr7:77004373 C>T did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:15497904 T>C did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr22:32015654 A>G maps to ENST00000422296 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr12:123471964 C>T maps to NM_020845.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr10:3208517 C>T maps to ENST00000380989 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr12:130847319 A>C maps to NM_004764.4 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr7:47851484 G>T maps to NM_138295.3 S2504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr7:47886535 C>T maps to NM_138295.3 E1698E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0891-01A-01W-0420-08 chr16:81253840 G>A maps to NM_052892.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr10:102057173 G>T maps to NM_016112.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr10:102056811 C>T maps to NM_016112.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr5:137226194 C>A maps to ENST00000230643 Y19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr22:46654128 G>A maps to NM_006071.1 F1697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr6:51890437 C>A maps to NM_138694.3 R1390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr6:51524030 A>G maps to NM_138694.3 Y3631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr6:51882329 C>T maps to NM_138694.3 A1826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr6:51701200 C>A did not map to a codon.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr8:110535076 G>A maps to ENST00000426474 Q4097Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr8:110504191 T>G maps to ENST00000426474 L3402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0934-01A-02W-0420-08 chr8:110455223 C>T maps to ENST00000426474 S1481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr8:110457674 C>T maps to ENST00000426474 G1859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr8:79510669 A>C maps to NM_181839.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr11:125300008 G>A maps to NM_022062.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:159519564 A>T maps to NM_003628.3 K790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr2:159519467 G>C maps to NM_003628.3 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr2:159433806 C>T maps to NM_003628.3 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr2:159481793 G>A maps to NM_003628.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr10:74701080 G>A maps to NM_032562.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr16:68283280 C>T maps to NM_012320.3 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr19:48603005 G>T maps to NM_003706.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1350-01A-01W-0490-10 chr15:42377336 C>T did not map to a codon.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr15:42442883 G>C maps to ENST00000397272 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr2:160889590 G>A maps to NM_007366.4 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr2:160833793 C>T did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:133700431 T>A did not map to a codon.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr11:59811020 G>A maps to NM_173801.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr4:84026173 C>A did not map to a codon.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr20:30784385 G>A maps to NM_002657.3 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr11:64031526 C>T maps to NM_000932.2 H865H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr20:9346156 A>C maps to NM_001172646.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr20:9440286 A>G maps to NM_001172646.1 K1026K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr17:43194019 G>C maps to NM_133373.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr10:95791573 C>T maps to ENST00000371380 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr16:81942085 G>A maps to NM_002661.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr3:155215195 G>A maps to ENST00000340059 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr2:198950442 A>G maps to NM_006226.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr2:198950031 C>T maps to NM_006226.3 Y597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr3:17052694 T>G maps to NM_001144382.1 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr5:41313738 C>A maps to NM_001005473.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr3:171362743 G>T maps to NM_002662.3 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr3:171338239 T>C maps to NM_002662.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr3:171427393 T>A maps to NM_002662.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr17:4711105 C>T maps to NM_002663.3 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr17:4713273 G>A maps to NM_002663.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr19:40883998 C>T maps to NM_012268.2 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr1:242253344 T>G maps to NM_152666.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr2:68607904 A>T maps to NM_002664.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr2:68613643 C>A maps to NM_002664.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr14:67862144 G>A maps to NM_016445.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr2:179368484 A>G did not map to a codon.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr19:49344561 C>T maps to NM_020904.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1633-01A-01W-0615-10 chr11:16892689 C>T maps to ENST00000448080 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr11:73361655 G>T maps to NM_021200.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr6:151055100 C>G maps to NM_001029884.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr14:65199546 G>T maps to ENST00000394691 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr5:156194 G>T maps to NM_052909.3 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr2:43969962 C>A maps to NM_172069.3 S1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr2:43969966 G>A maps to NM_172069.3 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr2:208842236 C>T maps to NM_001080475.2 W228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr15:65157819 C>A maps to NM_025201.4 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr6:161139774 G>A maps to NM_000301.3 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr6:161152919 A>T maps to NM_000301.3 K528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr19:4511817 A>G maps to NM_001080400.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr20:21143059 G>A maps to NM_018474.4 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr1:12024279 C>T maps to ENST00000376369 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr1:12018661 C>T maps to ENST00000376369 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr7:100855615 G>A maps to NM_001084.4 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr23:103041610 C>T did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr23:114864145 G>A did not map to a codon.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr20:44538258 A>C maps to NM_006227.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr19:17487776 G>A maps to NM_031310.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr10:20534379 G>C maps to NM_032812.7 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr10:20290881 G>A maps to NM_032812.7 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr10:20534433 G>A maps to NM_032812.7 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr3:126748780 C>T maps to NM_032242.3 P1645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr3:126735404 C>T maps to NM_032242.3 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr23:153699458 G>A did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr23:153689043 A>T did not map to a codon.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr23:153692567 G>A did not map to a codon.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr7:131833363 C>A maps to NM_020911.1 E1568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr7:131817903 T>A maps to NM_020911.1 A1831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr7:131865461 C>T maps to NM_020911.1 G1174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr7:131829915 A>T maps to NM_020911.1 I1729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr3:48450874 C>G maps to NM_001130082.1 L1983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr22:50724252 C>T maps to NM_012401.2 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr23:153033786 G>A did not map to a codon.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr12:94641842 G>T maps to NM_005761.1 V851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr16:72174373 C>T maps to NM_031293.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr16:8895756 G>A maps to NM_000303.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr2:190708746 C>T maps to NM_000534.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr23:152936014 A>T did not map to a codon.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr2:219209529 G>A did not map to a codon.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr19:50367328 C>G did not map to a codon.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr10:118401646 A>G maps to NM_005396.4 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr14:74179712 G>A maps to NM_006029.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr23:152226779 C>A did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr23:152159719 T>C did not map to a codon.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr23:152159633 G>T did not map to a codon.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr19:46998641 C>T maps to NM_020709.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr19:46997543 C>T maps to NM_020709.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr17:37826359 A>T maps to NM_002686.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr23:7868838 A>T did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr19:7619515 C>T maps to NM_001166111.1 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr19:7621563 C>T maps to NM_001166111.1 N1088N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr12:89864230 C>T maps to NM_172240.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr23:24828031 A>G did not map to a codon.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr23:24732733 C>T did not map to a codon.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr23:24830876 G>T did not map to a codon.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr23:24767066 C>T did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr11:65036161 G>T maps to NM_002689.2 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr7:44157329 G>T maps to NM_006230.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr11:74303708 G>A maps to NM_006591.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr12:133220530 G>A maps to ENST00000455752 V1397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr18:51800323 C>A maps to NM_007195.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr5:74865202 T>C maps to NM_016218.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr7:44120511 G>A maps to NM_013284.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr4:2209782 G>A maps to NM_181808.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr3:121207400 T>A maps to ENST00000393672 I1595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr2:86255038 G>A maps to NM_015425.3 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr2:86258452 C>T maps to NM_015425.3 Q1526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr2:113325653 G>A maps to NM_019014.4 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr17:7416195 C>G maps to NM_000937.4 G1570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr3:184081349 C>T maps to NM_006232.2 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1525-01A-01W-0615-10 chr10:79777461 G>A maps to NM_007055.3 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr12:106757661 G>T maps to NM_018082.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr12:106895133 C>T maps to NM_018082.5 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr1:145608204 A>G maps to NM_006468.6 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr7:53103789 G>A maps to NM_182595.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr2:25387507 A>C did not map to a codon.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr9:134385307 G>T maps to NM_007171.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr14:77746807 T>A did not map to a codon.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr14:77762596 C>A maps to NM_013382.5 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr7:94989302 A>G maps to NM_000940.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr8:99169859 G>A maps to NM_015029.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr7:100304542 G>A maps to NM_005837.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr6:105606437 C>T maps to NM_022361.4 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr23:48369685 T>G did not map to a codon.
Sequencing variant TCGA-23-1026-01B-01W-0484-10 chr23:48374142 G>A did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr23:48375612 G>A did not map to a codon.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr13:38156559 G>A maps to NM_006475.2 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr13:38171406 A>G maps to NM_006475.2 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr21:14987795 G>T maps to NM_174981.3 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr21:14983061 G>A maps to NM_174981.3 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr2:130832769 G>A maps to NM_001099771.2 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr2:130833007 A>G maps to NM_001099771.2 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr2:130872528 G>C maps to NM_001099771.2 Y245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr11:120170352 G>A maps to NM_014352.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr11:120180220 C>T maps to NM_014352.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr2:105473035 G>A maps to NM_006236.1 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:82763381 T>A did not map to a codon.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr23:82763968 G>T did not map to a codon.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr9:4663148 C>G maps to NM_203453.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr9:134183658 C>A maps to NM_032728.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1350-01A-01W-0490-10 chr6:35392165 C>T maps to NM_006238.4 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr3:12458477 T>C maps to NM_015869.4 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr4:23816028 G>A maps to NM_013261.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr4:74853709 G>C maps to NM_002704.3 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr4:76797628 G>T maps to NM_006239.2 C377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr12:81747070 T>A maps to NM_003625.2 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr12:81719568 T>A maps to NM_003625.2 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1728-01A-01W-0699-08 chr12:81671099 T>A maps to NM_003625.2 I1102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr12:27807737 A>G maps to NM_003622.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr11:7661072 C>T maps to NM_003621.2 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr12:42729718 A>C maps to NM_016488.6 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr1:143767440 C>T maps to NM_001123068.1 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr2:170493408 A>G maps to NM_004792.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr2:170493378 A>G maps to NM_004792.2 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0927-01A-02W-0419-10 chr22:22036751 C>T maps to NM_148175.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr22:22039066 G>A maps to NM_148175.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr5:102482229 G>A did not map to a codon.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr16:4940196 C>T maps to NM_002705.4 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr16:4937134 C>T did not map to a codon.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr16:4935028 G>C maps to NM_002705.4 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr16:4935525 C>A maps to NM_002705.4 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr2:27605443 G>A maps to NM_177983.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr12:63087766 G>A maps to NM_020700.1 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr1:161140959 C>T maps to NM_001122764.1 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr6:30572407 G>A maps to NM_002714.2 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr14:104219372 C>T maps to NM_015316.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr1:204380341 C>A maps to NM_032833.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr7:113519907 T>A maps to NM_002711.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr7:113520111 A>G maps to NM_002711.3 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2109-01A-01W-0722-08 chr7:113519847 G>C maps to NM_002711.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr23:49142295 G>C did not map to a codon.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr23:49143087 A>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:49142460 C>A did not map to a codon.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr23:49143119 T>C did not map to a codon.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr2:242099842 T>C maps to NM_002712.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr2:242102755 C>T maps to NM_002712.1 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr5:133541779 G>A maps to NM_002715.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr4:6377560 C>T maps to NM_181876.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr4:6374373 G>T maps to NM_181876.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0889-01A-01W-0419-10 chr11:64699340 G>T did not map to a codon.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr11:64699077 G>A maps to NM_006244.3 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr4:102004362 G>C maps to NM_000944.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr9:127916196 G>A maps to NM_001123355.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr10:103897626 G>A maps to NM_015062.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr10:47087574 T>C maps to NM_005972.4 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr10:47087273 G>A maps to NM_005972.4 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr18:77710723 C>T maps to NM_025078.4 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr18:77679248 G>A maps to NM_025078.4 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr1:19644238 G>A maps to NM_017765.2 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr22:22890968 C>T maps to NM_206954.1 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr1:12856111 G>A maps to NM_023013.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr1:12837354 A>G maps to NM_001080830.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr1:12921600 G>A maps to NM_023014.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr1:12980139 G>A maps to NM_001012277.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr8:70978518 C>A maps to NM_024504.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr8:70967603 A>G maps to NM_024504.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr21:43221549 C>A maps to NM_022115.3 G1458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr1:3328713 C>T maps to NM_022114.3 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr1:14106983 C>T maps to NM_012231.4 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr4:121774643 G>T maps to NM_018699.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr16:90128463 C>T maps to NM_001098173.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr5:23527155 T>C maps to NM_020227.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr1:203453265 C>T maps to NM_201348.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr6:105736640 G>A maps to NM_002726.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr6:105821389 C>T maps to NM_002726.4 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr6:105771644 T>G did not map to a codon.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr10:72357808 T>A maps to NM_005041.4 *556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr1:186266036 G>T maps to NM_005807.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr20:62197090 G>A maps to NM_001037335.2 D1028D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr12:42853780 C>A maps to NM_153026.2 G776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr3:64084735 G>A maps to NM_198859.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr3:64085269 G>T maps to NM_198859.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:57159471 G>C maps to NM_006252.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr12:49398331 G>C maps to NM_002733.3 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr3:48828035 G>A maps to NM_004157.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr17:64800029 C>T maps to NM_002737.2 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr17:64782998 T>G maps to NM_002737.2 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr16:24202410 C>T maps to NM_002738.6 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1627-01A-01W-0615-10 chr16:23999886 C>T maps to NM_002738.6 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr2:46207450 C>T maps to NM_005400.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr2:46228561 C>T maps to NM_005400.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr19:54407995 G>A maps to NM_002739.3 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0927-01A-02W-0419-10 chr10:6533663 C>A maps to NM_006257.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr10:6504277 C>A maps to NM_006257.2 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2399-01A-01W-0799-08 chr14:30107927 C>G maps to NM_002742.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr14:30047501 G>T maps to NM_002742.2 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr14:30068313 C>T maps to NM_002742.2 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr19:47207424 C>G did not map to a codon.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr19:47197270 G>A maps to ENST00000449438 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr19:47217201 G>A maps to ENST00000449438 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr8:48805846 C>T maps to NM_006904.6 S1233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr10:53822294 A>T did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr4:82031735 C>A maps to NM_006259.1 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr4:148594892 A>T maps to NM_138364.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr21:48078802 C>T maps to NM_206962.1 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr21:48064294 C>T maps to NM_206962.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr12:3702269 C>T maps to NM_019854.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr2:68882440 C>T maps to NM_138964.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr20:5294721 G>A maps to NM_144773.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr2:95940494 T>G maps to NM_144707.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0934-01A-02W-0420-08 chr1:214170264 C>T maps to NM_002763.3 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr14:75329536 A>T maps to ENST00000445876 L334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr11:60668819 C>A maps to NM_014502.4 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr1:150316936 A>T maps to NM_004698.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr19:54628016 C>T maps to NM_015629.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr6:4032297 C>T maps to NM_003913.4 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr20:62632581 T>A maps to NM_012469.3 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr20:62630982 C>A maps to NM_012469.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr20:62624828 A>C maps to NM_012469.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1728-01A-01W-0699-08 chr17:1563791 G>A maps to NM_006445.3 L1573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr17:74309052 C>T maps to NM_002766.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr2:240982348 G>C maps to NM_001080835.1 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr12:10999789 G>A maps to NM_007244.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr23:37285166 A>G did not map to a codon.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr23:150869190 A>T did not map to a codon.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr23:150869495 T>G did not map to a codon.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr23:150869328 A>T did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr7:141536935 C>T maps to NM_001008270.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr15:56032826 G>A maps to NM_173814.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr19:847908 C>T maps to NM_002777.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr1:151001308 C>A maps to NM_021222.1 C274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0934-01A-02W-0420-08 chr19:40902611 C>T maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr5:139189189 G>A maps to NM_032289.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr5:139193781 A>T maps to NM_032289.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr8:18729614 G>A maps to ENST00000440756 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr2:113951509 C>G maps to NM_012455.2 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr19:36237708 G>C maps to NM_172341.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr19:43702147 C>G did not map to a codon.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr19:43679400 C>T maps to ENST00000270059 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr19:43679475 C>T maps to ENST00000270059 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr7:42964386 C>T maps to NM_002787.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr14:58711652 C>G maps to NM_002788.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1626-01A-01W-0615-10 chr1:151373046 C>G maps to NM_002796.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr17:4701624 C>T maps to NM_002798.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr14:90726457 G>A did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr11:47445637 G>A maps to NM_002804.4 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr11:47441884 C>A maps to NM_002804.4 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr17:40725172 C>G maps to NM_016556.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr19:40485748 G>A maps to NM_006503.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr17:61908173 G>A maps to NM_002805.5 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr2:231926009 G>T maps to NM_002807.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr23:107328301 C>T did not map to a codon.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr17:30791555 G>A maps to NM_002815.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr2:54128636 A>G maps to NM_014614.2 D1045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr20:1145090 C>A maps to NM_006814.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr7:56079454 T>A maps to NM_004577.3 *226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr10:124740040 C>A maps to NM_153336.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2409-01A-01W-0799-08 chr2:86352129 C>T maps to NM_017952.5 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:45297699 T>A maps to NM_003738.4 K158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr23:23411369 A>G did not map to a codon.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr23:23411776 G>T did not map to a codon.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr23:23411675 G>A did not map to a codon.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr23:23397857 C>A did not map to a codon.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr23:23412061 G>C did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr10:27692186 C>T maps to NM_001034842.3 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr10:27692272 G>T maps to NM_001034842.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr11:479121 C>A maps to NM_030783.1 Y135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr10:89711872 A>C did not map to a codon.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr10:16528616 G>C did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr9:139874449 C>A maps to ENST00000224167 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr9:139872143 G>A maps to ENST00000224167 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:79002108 G>T maps to NM_000959.3 G273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr14:74343822 A>T maps to NM_152444.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr1:186643622 C>T maps to NM_000963.2 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr11:13513969 A>G maps to NM_000315.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1026-01B-01W-0484-10 chr8:141829026 C>A maps to NM_005607.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr8:141771319 G>A maps to NM_005607.4 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr8:27303405 G>T maps to NM_004103.3 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr20:62163957 G>A maps to NM_005975.2 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr9:96864017 T>A maps to ENST00000434261 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr12:112926906 A>T maps to ENST00000392596 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr1:214638125 G>A maps to NM_005401.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr14:88936358 G>C maps to NM_007039.3 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr14:88945476 G>A maps to NM_007039.3 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr14:88967713 T>C did not map to a codon.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr3:47450464 C>T maps to NM_015466.2 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr2:120567545 T>A maps to NM_002830.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr9:8484339 A>G maps to NM_002839.3 D1064D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr9:8497240 C>A did not map to a codon.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr10:129871626 C>T maps to NM_006504.4 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr1:44075158 C>G maps to NM_002840.3 Y1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr1:44069378 C>T maps to NM_002840.3 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr3:61734582 C>T maps to NM_002841.3 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1565-01A-01W-0551-08 chr3:62189577 C>T maps to NM_002841.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr19:55710053 C>T maps to NM_002842.3 R549R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr6:128505585 T>A maps to ENST00000368210 K385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr6:128297858 A>T maps to ENST00000368210 S1322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr2:220164813 G>A maps to NM_002846.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr2:220162005 G>A maps to NM_002846.3 C679C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr2:220162762 C>G maps to NM_002846.3 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:220164465 C>A maps to NM_002846.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr7:157387959 C>T maps to NM_002847.3 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr7:157387980 C>T maps to NM_002847.3 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr7:157361627 G>A maps to NM_002847.3 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr7:157926523 G>A maps to NM_002847.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr12:15661550 C>T maps to NM_030667.1 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr12:15654719 G>A maps to NM_030667.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr12:15654947 C>A maps to NM_030667.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr20:40727183 C>T maps to ENST00000373198 K1263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr20:40877325 C>T did not map to a codon.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr20:40770603 G>A maps to ENST00000373198 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr20:41385101 C>A maps to ENST00000373198 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr7:121651098 G>T maps to NM_002851.2 G667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr7:121652840 G>A maps to NM_002851.2 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr7:121651514 G>A maps to NM_002851.2 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr2:20494169 T>C maps to ENST00000361078 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr12:132414547 C>T maps to NM_025215.5 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr2:61180217 C>A maps to NM_144709.2 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr7:99817607 C>A maps to NM_024070.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr21:45547957 C>T maps to NM_005049.2 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:1680796 G>C maps to NM_012293.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr2:1652437 G>A maps to NM_012293.1 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr8:52284520 G>T maps to NM_144651.4 V1271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr3:58368239 G>T did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr12:120662172 C>A maps to NM_001080855.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr14:51410968 G>A maps to NM_002863.4 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr12:9355157 G>A maps to NM_002864.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr6:163984626 A>T maps to ENST00000361752 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr3:49069659 T>C maps to NM_198880.1 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr17:74278121 C>T maps to NM_032134.1 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:180165664 C>T maps to NM_002826.4 D579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr1:180163346 G>C did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr3:113795661 C>T maps to ENST00000485050 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr8:37729628 G>A maps to NM_001002814.2 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr8:37720445 C>T maps to NM_001002814.2 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr2:73303219 G>A maps to NM_015470.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr15:55520899 A>G maps to NM_183235.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr22:23492251 G>A maps to NM_004914.2 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr19:11446126 G>A maps to NM_004283.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr2:135926293 C>T maps to NM_001172435.1 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr2:135908054 C>T maps to NM_001172435.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr2:135911446 G>T did not map to a codon.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr23:102192278 C>T did not map to a codon.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr23:69504159 A>G did not map to a codon.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr23:69502163 A>G did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr19:41289957 C>T maps to ENST00000419646 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr23:13727277 C>T did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr23:13727390 G>A did not map to a codon.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr17:5286418 G>A maps to NM_004703.4 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr9:125751632 C>T maps to NM_012197.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr9:125746948 A>C maps to NM_012197.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr9:125746912 C>G maps to NM_012197.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr7:66270244 T>C maps to ENST00000451741 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr1:76260325 A>G maps to NM_004582.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr1:202850282 G>A maps to NM_002871.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1471-01A-01W-0551-08 chr3:9005024 G>A maps to NM_020165.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1028-01A-01W-0484-10 chr15:41001311 C>T maps to NM_002875.4 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr2:17692184 C>T maps to NM_001099218.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr8:95479689 A>G maps to NM_012415.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr6:150240386 G>A maps to NM_001001788.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr1:155110533 G>A maps to NM_018845.3 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr9:135985877 T>C did not map to a codon.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr9:135982606 C>T maps to NM_006266.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr9:135979136 C>G maps to NM_006266.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1105-01A-01W-0484-10 chr20:32661418 A>T maps to NM_016732.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr7:45216941 A>T maps to NM_005856.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr16:67765390 G>A maps to NM_020850.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr5:170351441 A>G maps to NM_022897.3 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr5:170346476 T>G maps to NM_022897.3 Y378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr9:6014608 A>G maps to NM_012416.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr9:6013909 G>T maps to NM_012416.2 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr1:21943858 G>T maps to NM_001145658.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:21944444 T>G maps to NM_001145658.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0911-01A-01W-0420-08 chr4:99325730 T>C maps to NM_001100426.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr23:131348287 C>G did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr7:22165225 C>T maps to ENST00000344041 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr7:22347968 G>A maps to ENST00000344041 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr17:38349235 G>A maps to ENST00000456989 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr2:204306133 G>T maps to ENST00000374493 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr2:204304867 C>T maps to ENST00000374493 K1067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr3:25622183 C>T maps to NM_000965.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr3:25502768 C>A maps to NM_000965.3 C81*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-13-0765-01A-01W-0372-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr11:63312249 C>T maps to NM_004585.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr5:167929030 G>A maps to NM_002887.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr5:86681166 T>G maps to NM_002890.1 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr13:114780757 A>G maps to ENST00000389544 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr12:113568720 G>A maps to NM_001193520.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr1:178269207 G>T maps to ENST00000263528 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr15:79254511 G>A maps to NM_002891.4 R1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr20:4768358 G>A maps to NM_014737.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr1:206760174 C>A maps to NM_182663.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr13:49039373 C>T maps to NM_000321.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1635-01A-01W-0615-10 chr13:48951052 G>C did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr13:49027155 C>T maps to NM_000321.2 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr13:48881461 C>T maps to NM_000321.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr8:53555088 C>A maps to NM_014781.4 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr8:53586647 A>C maps to NM_014781.4 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr8:53555016 C>A maps to NM_014781.4 G1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr8:53555085 C>A maps to NM_014781.4 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr7:5103356 A>G maps to NM_021163.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr7:5103785 T>C maps to NM_021163.3 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1560-01A-01W-0615-10 chr16:24578490 C>T maps to NM_006910.4 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr16:24581308 C>T maps to NM_006910.4 Q1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr16:24582568 C>T maps to NM_006910.4 N1394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr23:16870700 G>A did not map to a codon.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr18:20602130 T>C maps to ENST00000360790 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1634-01A-01W-0615-10 chr2:28050538 C>T maps to NM_022128.1 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr20:35635837 G>A maps to NM_002895.2 Y949Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr20:35635837 G>A maps to NM_002895.2 Y949Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr23:47028832 G>A did not map to a codon.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr20:34242047 T>C maps to NM_001198838.1 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr8:94746628 T>G maps to NM_203390.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr1:110888224 G>A maps to NM_022768.4 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr1:110883319 A>G maps to NM_022768.4 K431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr6:155153520 G>T maps to NM_014892.3 G936G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-13-1404-01A-01W-0494-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr14:73569919 C>G maps to NM_021239.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr14:73554799 C>T maps to NM_021239.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr13:79933777 T>G maps to ENST00000438737 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr13:79951642 C>T maps to ENST00000438737 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr5:145616963 A>G maps to NM_018989.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr23:48434993 T>G did not map to a codon.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr7:155537868 C>G maps to NM_053043.2 S851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr1:235324282 A>G maps to NM_015014.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr20:34309748 A>G maps to NM_184234.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr23:106312506 G>A did not map to a codon.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr4:40440556 G>C maps to NM_001098634.1 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr11:114273568 A>G maps to NM_016090.2 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr2:161349852 G>A maps to NM_016836.3 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr3:29476391 C>A maps to NM_001003793.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr23:135957726 T>C did not map to a codon.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr23:129543287 A>G did not map to a codon.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr4:26432337 C>T maps to NM_005349.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr8:30332299 G>C maps to NM_001008712.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr1:173953670 T>C maps to NM_172071.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:173941646 C>T maps to NM_172071.2 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr9:125642403 G>A maps to NM_001100588.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr13:49086004 G>A maps to NM_001268.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr19:50037524 C>T maps to NM_020650.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr14:103188668 T>G maps to NM_015156.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:211486185 G>A maps to NM_001136223.1 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr1:211469094 G>A maps to NM_001136223.1 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr1:211654727 G>A maps to NM_183059.2 N10N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr6:31922843 C>G maps to ENST00000375425 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr19:55556576 G>C maps to NM_001145971.1 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr19:10132083 C>T maps to NM_015725.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr9:36112345 C>T maps to NM_021111.2 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr12:21643148 T>G maps to NM_032941.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr1:120345693 G>T maps to NM_032044.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:120337248 G>A maps to NM_032044.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr2:61144021 A>G maps to NM_002908.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr19:45535915 C>G maps to ENST00000221452 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr7:103301821 C>T did not map to a codon.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr7:103179741 C>T maps to ENST00000428762 T2321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr23:153207036 G>T did not map to a codon.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr23:153205627 A>G did not map to a codon.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr23:17088086 C>A did not map to a codon.
Sequencing variant TCGA-61-2088-01A-01W-0722-08 chr12:15262109 C>T maps to NM_032918.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr10:43622099 G>A maps to NM_020975.4 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr10:43619214 C>T maps to NM_020975.4 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr19:7734746 C>T maps to NM_020415.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr2:100020218 C>G maps to NM_016316.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr2:100055282 C>T maps to NM_016316.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1576-01A-01W-0615-10 chr4:39301642 G>A maps to ENST00000381897 Q937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr12:118456888 C>T maps to NM_007370.4 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr3:16358729 G>A maps to NM_015150.1 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr2:198540074 G>A maps to NM_144629.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr1:175956111 A>G maps to NM_022457.5 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr19:14077443 C>A did not map to a codon.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr9:3225131 G>A maps to NM_134428.1 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr1:151315399 G>A maps to NM_000449.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr6:117237422 C>T maps to NM_173560.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr19:19310020 C>T maps to NM_003721.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr13:37394091 G>T maps to NM_000538.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr23:109694908 C>A did not map to a codon.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:109696862 A>C did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:109696543 C>A did not map to a codon.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr23:109696286 T>C did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:109697237 G>A did not map to a codon.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr23:71351054 G>A did not map to a codon.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr23:71350665 C>T did not map to a codon.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr1:183816731 A>G maps to NM_015149.3 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr19:11527319 C>T maps to NM_001161616.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr19:11508183 C>T maps to NM_001161616.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr19:11526797 C>T maps to NM_001161616.1 W151*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-23-1022-01A-02W-0488-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr5:73069740 C>T maps to NM_001080479.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr5:73142290 A>G maps to NM_001080479.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr2:107075743 A>G maps to ENST00000304514 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr2:108478192 G>A maps to NM_182588.2 K734K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr2:108477647 A>G did not map to a codon.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr10:86008737 G>A maps to ENST00000358110 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr10:86012655 C>T maps to ENST00000358110 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr1:182571205 G>A maps to NM_002928.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:182569474 G>A maps to NM_002928.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr1:192128427 T>G maps to NM_130782.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr1:192780141 G>A maps to NM_002923.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr8:54871008 T>C maps to NM_170587.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr8:101075774 A>T maps to NM_015668.3 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr9:116224455 C>T maps to NM_144488.4 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr1:241262053 G>A maps to ENST00000407727 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr5:63802570 C>T maps to NM_001029875.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr16:109278 G>A maps to NM_022450.3 Y654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr17:74468866 C>T maps to NM_024599.5 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr1:156347188 C>T maps to NM_020407.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr8:22864558 C>T maps to NM_001160036.1 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr1:113245196 G>C maps to NM_175744.4 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr23:119211185 C>T did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:119293026 G>A did not map to a codon.
Sequencing variant TCGA-25-2408-01A-01W-0799-08 chr5:38952517 T>C maps to ENST00000296782 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr5:38947494 C>T maps to ENST00000296782 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr5:39002638 A>G maps to ENST00000296782 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr2:152314272 A>G did not map to a codon.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr2:152325065 G>C did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr17:1549750 G>A maps to NM_031430.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr12:130926552 G>T maps to NM_015347.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr22:20458523 C>A maps to NM_015672.1 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr6:72984123 G>A maps to NM_014989.4 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr6:72968727 T>C maps to NM_014989.4 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr8:104973341 T>C maps to NM_001100117.2 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr8:104709457 C>T maps to NM_001100117.2 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr20:19981349 C>T maps to ENST00000255006 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr20:19956237 G>A maps to ENST00000255006 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr7:105187419 T>G maps to NM_021930.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr6:7395356 T>C maps to NM_031480.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr14:24806667 T>A did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr21:43161429 C>T maps to ENST00000352483 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr18:40695394 T>G maps to NM_002930.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr15:89758443 G>T maps to NM_000326.4 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr1:40627308 G>T did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr23:73812799 C>A did not map to a codon.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr23:73811647 G>A did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:73815785 T>C did not map to a codon.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr9:5339623 G>A maps to NM_006911.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr16:67680614 A>T did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr5:177571006 C>T maps to NM_022762.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr14:21052339 G>A maps to NM_145250.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr2:3597982 G>A maps to NM_002936.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr15:59344630 G>T did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr17:19318108 G>T maps to NM_007148.4 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr20:48558182 C>T maps to NM_018683.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr11:71693955 C>G maps to NM_018320.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr23:106034426 A>G did not map to a codon.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr23:106016294 G>C did not map to a codon.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr2:7137069 A>C maps to NM_014746.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr5:158588282 G>A maps to NM_144726.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr4:141889013 G>A maps to NM_020724.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr21:30315999 A>G maps to NM_015565.2 H1449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr21:30304905 C>T maps to NM_015565.2 L1698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr13:25374503 A>T maps to ENST00000381927 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr6:13978054 T>C maps to NM_001165033.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr22:31600475 T>A maps to NM_152267.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr9:104307064 G>A maps to NM_019592.5 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr9:104302595 C>T maps to NM_019592.5 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr17:78265424 A>G did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr17:78237542 C>T maps to NM_020914.4 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr17:78320333 G>A maps to NM_020914.4 L2782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr11:119206995 G>A maps to NM_032015.3 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr6:37358530 C>T maps to NM_003958.3 F485F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-13-0791-01A-01W-0372-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr1:201970791 T>A maps to NM_020216.3 Y441*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-04-1347-01A-01W-0488-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr3:78666808 G>A maps to NM_002941.3 R1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr16:4851544 C>T maps to NM_024589.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr3:123695815 G>C maps to NM_017578.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr1:64624823 C>T maps to NM_005012.2 H445H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1584-01A-01W-0615-10 chr9:77286721 G>T maps to ENST00000396204 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr6:117710594 G>T maps to NM_002944.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr6:117724349 G>A maps to NM_002944.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr6:117710738 G>A maps to NM_002944.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr8:55541829 G>T maps to NM_006269.1 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr8:55533783 T>G maps to NM_006269.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr8:10466879 G>T maps to NM_178857.5 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:46719514 C>T did not map to a codon.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr23:96139483 G>T did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:96139556 C>T did not map to a codon.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr15:41816445 G>C maps to NM_015540.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr23:38135963 G>A did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr23:38145033 C>G did not map to a codon.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr23:38182166 G>C did not map to a codon.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr23:38182663 C>A did not map to a codon.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr14:21793542 G>T did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr14:21794270 C>A maps to NM_020366.3 G883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr12:113303275 C>T maps to NM_001143854.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr3:23960899 G>T maps to NM_002948.2 G175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr8:99057244 G>C maps to NM_000989.2 Y31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr3:12880848 T>A maps to ENST00000273223 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr9:127620286 C>T maps to NM_007209.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1322-01A-01W-0494-09 chr2:217364706 C>T maps to NM_000998.4 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr16:2002993 C>T maps to NM_005061.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr12:120635196 A>G maps to NM_053275.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr20:35862445 C>T maps to NM_002951.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr6:30314293 C>A maps to ENST00000412529 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr10:15145375 G>T maps to NM_183005.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr6:4999007 C>T maps to NM_006638.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1728-01A-01W-0699-08 chr18:33606958 C>T maps to NM_018170.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr6:34392998 C>A did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr4:152024192 G>A maps to NM_001006.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr6:166833416 C>T maps to ENST00000510118 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr23:20194458 T>C did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr23:20185832 T>C did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr23:83351222 G>A did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr17:57970679 G>A maps to NM_003161.2 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1634-01A-01W-0615-10 chr1:213403884 A>T maps to NM_012424.3 K364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr14:75373785 T>C maps to NM_031464.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr1:45243433 C>T maps to NM_001012.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr19:50140342 G>C maps to NM_006270.3 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr20:17602520 T>C maps to ENST00000377813 E1073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr6:7230383 C>T maps to NM_001003699.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr6:7230839 G>C maps to NM_001003699.3 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr6:7231271 T>G maps to NM_001003699.3 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr23:18662573 G>C did not map to a codon.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr23:18660212 A>C did not map to a codon.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr17:48562146 T>A maps to NM_018346.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr11:77451975 G>A maps to NM_016578.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr15:55475540 G>A maps to NM_016304.2 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr21:43892957 T>C maps to NM_080860.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr21:43912880 T>G maps to NM_080860.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr21:43913111 G>C maps to NM_080860.2 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr19:46303753 G>C maps to NM_030785.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr8:109001329 T>A maps to NM_178565.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr16:57261339 T>A maps to NM_133368.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr12:123006785 T>A maps to NM_023012.5 K23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr22:23401714 G>A maps to NM_014433.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr15:41767962 A>G maps to NM_015138.4 E476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr19:45992120 G>A maps to NM_005619.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr2:55214835 T>C did not map to a codon.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr11:57235181 G>T maps to NM_178570.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr3:186917743 G>A maps to NM_153708.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr3:46539650 T>A maps to NM_031440.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2088-01A-01W-0722-08 chr3:46542041 C>T maps to NM_031440.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr21:36164572 G>A maps to NM_001754.4 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr8:92972687 G>A maps to NM_175634.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr8:93026878 G>T maps to NM_175634.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr6:45480091 C>A maps to ENST00000359524 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1633-01A-01W-0615-10 chr9:137313651 G>T did not map to a codon.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr6:33165605 C>T maps to ENST00000374685 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr19:39008209 C>T maps to NM_000540.2 G3299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr19:39075641 C>T maps to NM_000540.2 I4902I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr19:38964115 C>A maps to NM_000540.2 R1289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr19:38968432 C>T maps to NM_000540.2 H1459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr19:38964345 A>T maps to NM_000540.2 G1365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1477-01A-01D-0472-08 chr1:237494209 T>C maps to NM_001035.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr1:237965197 A>T maps to NM_001035.2 G4711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr1:237947293 C>T maps to NM_001035.2 I4094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr1:237870247 G>A did not map to a codon.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr1:237778046 A>G maps to NM_001035.2 A1873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr15:33893657 G>T maps to NM_001036.3 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr15:33895398 C>T maps to NM_001036.3 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr1:153507755 G>T maps to NM_014624.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr1:153410739 T>C maps to NM_001045479.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:153333313 A>C maps to NM_002965.3 *115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr3:45751048 T>C maps to NM_014016.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr13:23911438 G>A maps to NM_014363.4 I2192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr13:23913132 G>A maps to NM_014363.4 Q1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr23:134992666 G>A did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr23:134993361 A>T did not map to a codon.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr14:21990978 C>T maps to NM_005407.1 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr14:21991568 C>A maps to NM_005407.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr18:76753292 G>A maps to NM_171999.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr6:130536360 C>A maps to ENST00000457563 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr14:55226943 G>A maps to NM_015589.4 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr3:169644856 C>G maps to NM_182610.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr7:92731856 G>C maps to NM_017654.3 S1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr7:92761354 C>T maps to NM_152703.2 L1310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr7:92763519 G>A maps to NM_152703.2 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr7:92761212 C>A maps to NM_152703.2 E1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr7:92761516 G>A maps to NM_152703.2 H1256H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr21:15870795 G>A maps to ENST00000285670 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr2:128757375 G>A maps to NM_001145928.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr13:21715101 T>C maps to NM_005870.4 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr4:174292632 C>A maps to NM_003864.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr17:73698615 C>T maps to NM_013260.6 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr22:50869810 C>T maps to ENST00000216061 H445H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr22:50857871 C>T maps to ENST00000216061 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr1:109771017 G>A maps to ENST00000369923 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1633-01A-01W-0615-10 chr23:128921962 C>A did not map to a codon.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr23:128926971 C>T did not map to a codon.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr3:18391168 C>T maps to ENST00000332610 Q629Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr3:18436358 G>C maps to ENST00000332610 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr3:18390871 C>T maps to ENST00000332610 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr2:200137335 C>T maps to NM_001172509.1 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr2:200137014 G>A maps to NM_001172509.1 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr23:84362524 G>A did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr19:36017692 C>A maps to NM_001166034.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr11:121177110 C>T maps to NM_001024956.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr19:50154344 C>A maps to NM_021228.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr1:155226122 G>A maps to NM_005698.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr6:28543041 T>A maps to NM_052923.1 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr6:28540481 A>G maps to NM_052923.1 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr6:28540553 A>G maps to NM_052923.1 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr4:83626507 C>T maps to NM_001037582.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr4:83557768 G>A maps to NM_001037582.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr2:224462650 C>T maps to NM_003469.4 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr15:51973987 G>C maps to NM_013243.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr11:61959642 A>C maps to NM_006552.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr7:12668846 G>A maps to NM_001112706.2 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr7:12691501 G>T maps to NM_001112706.2 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr2:239003058 A>C did not map to a codon.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr23:17768146 G>A did not map to a codon.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr23:18264895 T>C did not map to a codon.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr3:38802217 G>A maps to NM_006514.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr3:38835276 G>A maps to NM_006514.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr3:38770223 G>A maps to NM_006514.2 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr3:38892068 C>T maps to ENST00000302328 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr3:38921581 G>C maps to ENST00000302328 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr2:166852521 C>T did not map to a codon.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr2:166900451 G>A maps to NM_001165963.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr2:166852528 T>A maps to NM_001165963.1 R1525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr2:166892743 T>A maps to NM_001165963.1 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr2:166897911 C>T maps to NM_001165963.1 W748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr2:166903281 G>A maps to NM_001165963.1 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1525-01A-01W-0615-10 chr2:166170617 G>A maps to NM_001040142.1 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr2:166170590 G>A maps to NM_001040142.1 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1627-01A-01W-0615-10 chr2:166198804 G>A did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr11:118047101 C>A maps to NM_004588.4 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr2:166011144 T>A maps to NM_006922.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr2:165947487 G>A maps to NM_006922.3 D1725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr2:165952155 A>G maps to NM_006922.3 V1432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr2:165947801 G>A maps to NM_006922.3 R1621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr2:165947013 G>A maps to NM_006922.3 P1883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr17:62024485 C>T maps to NM_000334.4 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0928-01A-02W-0419-10 chr3:38651336 G>T maps to NM_001099404.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr3:38627205 A>G maps to NM_001099404.1 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr3:38618269 G>A maps to NM_001099404.1 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr3:38592051 G>A maps to NM_001099404.1 S1937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr12:52200804 G>A maps to NM_014191.2 L1845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr12:52184246 G>C maps to NM_014191.2 L1495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr2:167128929 C>T maps to ENST00000303354 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr2:167094660 A>G maps to ENST00000303354 Y1249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr16:23390079 C>A maps to ENST00000307331 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2016-01A-01W-0722-08 chr16:23391923 G>C maps to ENST00000307331 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr1:1225673 G>A maps to NM_001130413.2 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr8:144895095 G>A maps to NM_182706.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr22:43614425 G>A maps to NM_173050.2 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr1:31349815 C>T maps to NM_014654.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr1:31346168 C>A maps to NM_014654.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr11:61205107 G>T maps to NM_017841.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr1:161284213 A>C maps to NM_003001.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr7:4116654 C>T maps to NM_152744.3 Y1012Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr7:4050613 G>T maps to NM_152744.3 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr7:4089016 C>T maps to NM_152744.3 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr17:71384150 C>T maps to NM_001144952.1 P1406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr17:71361403 G>A maps to NM_001144952.1 P1766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr2:192711270 C>T maps to NM_004657.5 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr17:75190859 A>G maps to NM_001039573.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr1:177911037 G>T maps to NM_033127.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr14:39561750 T>C maps to NM_006364.2 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr4:110427527 G>A maps to NM_006323.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr10:75511002 T>A did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr4:83742213 C>G maps to ENST00000505472 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr4:83770049 C>T maps to ENST00000505472 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr6:108246056 C>A maps to NM_007214.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr9:91943767 A>G maps to NM_024077.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr20:13830202 T>C maps to NM_025229.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr1:169701924 T>A maps to NM_000450.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr1:169572291 G>A maps to NM_003005.3 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr15:101812978 G>C maps to NM_018445.4 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr7:80432077 C>G maps to NM_006379.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr7:84651725 A>G maps to NM_152754.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1517-01A-01W-0615-10 chr7:83037702 G>A maps to NM_012431.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr7:83119471 T>C maps to NM_012431.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1627-01A-01W-0615-10 chr1:156131243 C>T maps to NM_022367.3 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr5:9066611 C>T maps to NM_003966.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr5:9224933 C>T maps to NM_003966.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr3:122634452 G>T maps to NM_001031702.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr3:122632160 C>T maps to NM_001031702.2 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1633-01A-01W-0615-10 chr3:122642538 G>A maps to NM_001031702.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr3:122641230 G>A maps to NM_001031702.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr5:115840592 A>C maps to ENST00000257414 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr1:151107652 A>G maps to NM_001178061.1 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr3:101085489 G>A maps to NM_020654.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr3:101080584 T>A maps to NM_020654.3 K533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr3:101050937 G>A maps to NM_020654.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr15:72432488 T>A maps to NM_145204.3 C175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr1:26135162 T>A maps to NM_020451.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr1:26127533 G>T maps to NM_020451.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr5:132098187 G>A maps to NM_001098811.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr17:75484370 A>T maps to NM_001113491.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr1:67895854 C>T maps to NM_001018067.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr20:43132513 G>A maps to NM_006811.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr14:94849403 G>A maps to NM_001127707.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr14:94756558 G>T maps to NM_001100607.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr14:95030121 C>A maps to NM_006215.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr18:61260155 C>T maps to NM_012397.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr18:61570358 C>T maps to NM_001143818.1 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr18:61564440 G>C maps to NM_001143818.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr18:61325750 C>A maps to NM_006919.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr18:61324220 C>A did not map to a codon.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr18:61326647 C>T maps to NM_006919.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr18:61310703 T>C maps to NM_002974.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr6:2959419 G>A maps to ENST00000316782 T82T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-29-1777-01A-01W-0639-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr11:75277633 C>G maps to NM_001235.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr2:64863626 C>A maps to NM_014755.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr1:210415498 C>G maps to NM_019605.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr1:28601439 C>T maps to NM_031459.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr1:28599183 C>T maps to NM_031459.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr16:30982880 G>T maps to NM_014712.1 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr16:30976944 C>T maps to NM_014712.1 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr16:30982963 G>T maps to NM_014712.1 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr16:30991351 C>G maps to NM_014712.1 Y1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr16:30974874 G>C maps to NM_014712.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr3:47163178 C>A maps to NM_014159.6 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr3:47098745 A>T maps to NM_014159.6 Y2176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr3:9512591 G>A maps to ENST00000407969 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr3:9517426 T>C maps to ENST00000407969 S1346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr3:9512489 A>G maps to ENST00000407969 G1043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr12:123892120 C>T maps to NM_020382.3 H310H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr1:150915105 G>C maps to NM_001145415.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr9:135203567 T>C maps to ENST00000372169 E1139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr22:26736598 G>A did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr22:26747079 C>T maps to NM_021115.4 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr22:26693011 C>T maps to NM_021115.4 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr22:30742389 T>A maps to NM_005877.4 K102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1027-01A-02W-0486-08 chr2:198257818 C>T maps to NM_012433.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr11:65829173 A>G maps to NM_006842.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1546-01A-01W-0615-10 chr19:19427282 G>A maps to NM_172231.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr19:19414217 G>T maps to NM_172231.2 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1633-01A-01W-0615-10 chr3:52960127 G>A maps to NM_016329.3 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr10:7239536 C>G maps to NM_001018039.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr10:7239545 C>T maps to NM_001018039.1 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr4:154702674 C>G maps to NM_003013.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr1:70716464 G>T maps to NM_004768.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr19:19135920 C>A maps to NM_001017392.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1684-01A-01W-0633-09 chr6:99852477 C>T did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr11:94801043 C>T maps to NM_032102.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr12:132283984 C>T maps to NM_004592.2 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr10:104486512 G>A maps to NM_178858.4 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr10:120920466 G>C maps to NM_213649.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr17:48247634 C>A maps to NM_000023.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr8:13948086 A>T maps to NM_139167.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1350-01A-01W-0490-10 chr3:153943691 A>G maps to NM_015595.3 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr3:153840375 G>T maps to NM_015595.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2016-01A-01W-0722-08 chr1:67154921 A>T maps to ENST00000237247 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr8:8197042 G>A maps to NM_001080826.1 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr15:77425526 C>T maps to NM_024776.2 K1299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr10:52071163 G>A maps to ENST00000361543 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr2:201399858 G>T maps to NM_152524.5 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr2:201399818 A>G maps to NM_152524.5 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr22:25243734 C>T maps to NM_001039948.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr17:2276755 C>T maps to NM_014853.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr23:123504069 T>C did not map to a codon.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr1:156779282 C>T did not map to a codon.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr2:85662567 G>A maps to NM_198482.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1644-01B-01D-1526-09 chr23:80532587 G>T did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr23:80532535 A>G did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr2:235950810 G>A maps to NM_014521.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr2:235951005 G>A maps to NM_014521.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr2:235961312 G>A maps to NM_014521.2 E862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr3:15298554 G>A maps to NM_004844.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr19:4362367 G>A maps to NM_003025.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr5:171766347 C>A maps to NM_001017995.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr2:109964170 C>T maps to NM_001099289.1 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr11:70332557 G>A maps to ENST00000338508 N1274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr8:145153858 G>A maps to NM_030974.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr9:91690116 G>A maps to NM_016848.5 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr15:49160021 A>G maps to NM_203349.3 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr15:49135647 G>A maps to NM_203349.3 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr16:46615700 C>G maps to NM_024745.4 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr16:46629505 T>A maps to NM_024745.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr13:26620662 C>T maps to NM_001007538.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr19:41094994 C>T maps to NM_138392.3 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:9900270 G>C did not map to a codon.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:9841752 G>A did not map to a codon.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr23:9900828 C>T did not map to a codon.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr4:77676261 C>T maps to NM_020859.3 S1542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr23:50381260 A>T did not map to a codon.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr23:50378507 C>T did not map to a codon.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr16:48396300 G>C maps to NM_001006610.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr3:113327009 G>A maps to ENST00000393830 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr20:3674092 C>A did not map to a codon.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr20:3674874 G>A maps to NM_023068.3 D1083D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr19:50453486 G>A maps to NM_052884.2 Q613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr19:50461972 G>A maps to NM_052884.2 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr19:50461966 T>G maps to NM_052884.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr19:50462665 C>T maps to NM_052884.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr19:52003396 G>T maps to ENST00000441969 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1638-01A-01W-0639-09 chr19:52149591 C>T maps to ENST00000222107 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr19:52031042 T>C maps to NM_001245.5 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr19:51649163 T>C maps to NM_014385.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr19:51630491 C>T maps to NM_014441.2 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr11:116730108 G>A maps to ENST00000445177 R872R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr1:115323056 C>A did not map to a codon.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr12:56355484 T>G maps to NM_006928.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr21:38072126 C>A maps to NM_005069.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr14:72205844 A>G maps to NM_015556.1 T1794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr1:232650407 G>C maps to NM_020808.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr19:38610260 G>A maps to NM_015073.1 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr20:1915397 C>T maps to ENST00000400068 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr20:1532451 G>T maps to ENST00000381621 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr10:69647220 C>T maps to NM_012238.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr11:236208 A>T maps to NM_012239.5 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr19:4174679 C>T maps to NM_016539.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr17:79872211 G>T maps to NM_016538.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr14:61113246 G>A maps to NM_005982.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr19:46271384 G>A maps to NM_175875.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr18:47902253 C>T maps to NM_145060.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr3:170078892 T>C maps to NM_005414.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr6:31930760 G>A did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr5:54683920 A>G maps to NM_015360.4 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr5:36177065 G>C did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr8:134060175 C>T maps to NM_006748.3 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr1:160718305 T>A did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr13:103703767 C>T maps to NM_000452.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr13:103718246 C>T maps to NM_000452.2 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr13:103703608 G>C maps to NM_000452.2 Y253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:153716441 C>T did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr2:219254615 C>T maps to NM_000578.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr2:219259459 C>A maps to NM_000578.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr15:48539134 C>T maps to NM_000338.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr16:67995579 C>T maps to NM_005072.4 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr16:67979071 G>A maps to NM_005072.4 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr20:44682245 C>T maps to NM_001134771.1 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr20:44685811 C>T maps to NM_001134771.1 N1066N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr20:44678356 C>T maps to NM_001134771.1 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr3:124896803 G>T maps to NM_001195483.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr7:122763289 C>T did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr18:43262375 G>A maps to NM_007163.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr18:43243868 A>T maps to NM_007163.3 K491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr18:43221297 C>T maps to NM_007163.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr13:99378649 G>A maps to NM_005073.3 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr13:99362119 C>T did not map to a codon.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr2:230911025 C>T maps to NM_152527.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr2:230911220 C>A maps to NM_152527.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr2:230910734 G>T maps to NM_152527.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr23:73751289 G>A did not map to a codon.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr23:73745663 T>A did not map to a codon.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr1:110923658 C>T maps to NM_004696.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr12:60098799 G>T did not map to a codon.
Sequencing variant TCGA-61-1741-01A-02W-0639-09 chr12:60165105 C>T maps to NM_004731.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr10:61413431 C>T did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr10:61413886 A>G maps to NM_194298.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr6:25819365 G>C maps to NM_005074.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr6:25826700 C>G maps to NM_005074.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr6:25921481 G>T maps to NM_005835.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr11:22380985 C>T maps to NM_020346.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr19:49938042 G>A maps to NM_020309.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2540-01A-01D-1526-09 chr12:100806546 G>A did not map to a codon.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr2:228563704 C>A maps to NM_025243.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr11:35333939 C>A maps to NM_004171.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr5:36629574 C>T maps to NM_004172.4 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr19:15067394 G>A maps to NM_005071.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr19:15079173 C>T maps to NM_005071.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr19:15063750 C>A maps to NM_005071.1 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr19:15083683 G>A maps to NM_005071.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr1:53555485 G>C maps to NM_006671.4 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr8:42329815 G>A maps to NM_006749.3 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr8:42287610 C>T maps to NM_006749.3 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr11:63064805 T>C maps to NM_001039752.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr11:64323797 C>T maps to NM_018484.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr6:3287324 C>G maps to ENST00000436008 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr6:3273558 G>A maps to ENST00000436008 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr11:62997118 G>A maps to NM_199352.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr11:62747320 C>G maps to NM_004790.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr11:62751889 G>A maps to NM_004790.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr5:138715946 G>A maps to NM_152685.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr2:220034328 T>C maps to NM_001144890.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr20:19261696 C>T maps to NM_020689.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr14:92953020 C>T maps to NM_153646.3 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr14:92915420 C>T maps to NM_153646.3 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr22:19166129 C>T maps to NM_005984.2 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr23:129479158 C>A did not map to a codon.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr14:100759629 C>A did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:118587009 T>C did not map to a codon.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr23:118544162 G>A did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr23:118603983 G>A did not map to a codon.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr7:107342417 T>C maps to NM_000441.1 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0717-01A-01W-0370-10 chr7:103018943 G>A maps to ENST00000354356 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr7:103029840 G>A maps to ENST00000354356 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr8:92355654 A>T maps to NM_134266.1 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr8:92350461 T>G did not map to a codon.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr6:35927254 A>G maps to NM_052961.3 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr1:205897032 G>A maps to NM_134325.2 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr1:153750719 C>A maps to ENST00000271857 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr15:85438286 C>T maps to NM_004213.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr9:86900442 G>A maps to NM_022127.2 Y488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr20:45354907 C>T maps to NM_030777.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr22:24204382 G>A maps to NM_030807.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1586-01A-02W-0633-09 chr22:24224736 G>A maps to NM_030807.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr12:40223984 G>T maps to NM_052885.3 Y455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr12:7967094 G>A maps to NM_153449.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr12:8083912 C>T maps to NM_006931.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr12:8086489 T>C maps to NM_006931.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr9:130162196 C>G maps to NM_014580.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr4:9987353 C>T maps to NM_020041.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr4:9909888 C>A maps to NM_020041.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr4:9922140 C>G maps to NM_020041.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr1:101362170 G>A maps to NM_133496.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr4:42020140 C>T maps to NM_006345.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr3:155560289 G>A maps to NM_004733.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr3:155560337 G>A maps to NM_004733.3 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr23:48762606 C>A did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr6:44224593 C>T maps to NM_178148.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr6:8421050 A>C maps to NM_001142540.1 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr19:16677360 G>A maps to NM_024881.4 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr1:234367196 G>A maps to NM_173508.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr14:58063463 G>T maps to NM_001080455.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr5:150846758 G>C did not map to a codon.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr5:150715075 G>A maps to NM_181776.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr21:43984816 G>A did not map to a codon.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr11:124950578 C>A maps to NM_198277.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr11:118896778 G>T maps to NM_001164278.1 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr17:79250914 G>A maps to NM_001037984.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr2:165793873 T>A maps to ENST00000409662 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr23:48324675 G>A did not map to a codon.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr23:48318118 G>A did not map to a codon.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr23:48318130 G>C did not map to a codon.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr23:48317931 G>A did not map to a codon.
Alternatively spliced codon TCGA-13-0726-01A-01W-0372-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr16:58713976 A>G maps to NM_018231.1 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr16:84075621 C>T maps to NM_001080442.1 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr10:18276512 T>A maps to NM_001145195.1 L401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr14:21467685 C>T maps to NM_014579.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr3:125726055 G>A maps to NM_001008485.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr3:125725954 A>G maps to NM_017836.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr11:57182555 G>A maps to ENST00000428603 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr1:75684940 C>G did not map to a codon.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr5:33964005 G>A maps to NM_016180.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr8:142227243 G>A maps to NM_001080431.1 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr8:142222391 G>A maps to NM_001080431.1 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr17:19451411 C>T maps to ENST00000395585 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr17:19480785 C>A maps to ENST00000395585 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr17:42330612 G>A maps to NM_000342.3 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr17:42330582 G>T maps to NM_000342.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr20:3209862 C>T maps to NM_001174090.1 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr7:150769177 G>A maps to NM_003040.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr7:150771799 A>T maps to NM_003040.3 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr4:72412098 G>A maps to NM_001098484.2 W825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr3:27498165 T>C maps to ENST00000425128 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1105-01A-01W-0484-10 chr12:51888784 C>T maps to NM_001039960.1 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr12:51868221 G>T maps to NM_001039960.1 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr12:51868176 G>A maps to NM_001039960.1 W652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr22:32495225 C>G maps to NM_000343.3 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr17:18872682 C>T maps to NM_152351.3 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr16:24902340 G>T maps to NM_052944.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr16:24922748 C>G maps to NM_052944.2 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0730-01A-01W-0370-10 chr19:17992858 C>T maps to NM_000453.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr2:27430473 C>T maps to NM_021095.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr2:27427729 G>C maps to NM_021095.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr2:108622653 A>C maps to NM_021815.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr1:48705047 C>T maps to NM_001135181.1 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr1:48697696 C>A maps to NM_001135181.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr1:48690413 C>T maps to NM_001135181.1 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr3:11059655 C>T maps to NM_003042.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2436-01A-01D-1526-09 chr3:11067950 G>A maps to NM_003042.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1316-01A-01W-0494-09 chr3:10916710 G>A maps to NM_014229.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr23:115572241 G>C did not map to a codon.
Sequencing variant TCGA-61-1736-01B-01W-0722-08 chr23:115582750 G>T did not map to a codon.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr23:115588884 T>G did not map to a codon.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr5:1242839 C>T maps to NM_182632.2 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr16:55706076 G>T maps to NM_001043.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr16:55729188 G>T did not map to a codon.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr3:45801357 G>A maps to NM_020208.3 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr5:1401056 C>T maps to NM_001044.4 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr5:1441483 G>A maps to NM_001044.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr17:28545856 C>A maps to ENST00000394821 G188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr17:28548916 A>G maps to ENST00000394821 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr3:14508100 G>A maps to NM_001134367.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr23:152958572 C>A did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr1:44468303 C>T maps to NM_201649.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr3:170244653 G>T maps to NM_020949.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr3:170198579 C>T maps to NM_020949.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr3:170216488 C>T maps to NM_020949.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr23:70147770 G>T did not map to a codon.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr23:70145723 C>T did not map to a codon.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr22:21384503 C>G maps to NM_004173.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr14:23248048 G>C maps to NM_001126106.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr19:33355661 G>A maps to NM_014270.4 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr19:47935622 C>T maps to NM_015063.2 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr14:70633726 G>A maps to NM_183002.1 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:27427697 G>A maps to NM_003047.3 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr1:173545822 C>T maps to NM_178527.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr2:103281629 C>T maps to NM_003048.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr16:67288981 G>A maps to NM_004594.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr16:67298295 G>A maps to NM_004594.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:135092706 G>T did not map to a codon.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr23:135092656 C>T did not map to a codon.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr23:135106546 G>T did not map to a codon.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr23:46466492 G>A did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr23:46521557 T>G did not map to a codon.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr3:143212561 G>A maps to NM_173653.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr12:21453468 C>T maps to NM_134431.3 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr12:21054395 T>C maps to NM_019844.2 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr11:74907585 A>T maps to NM_007256.4 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr11:74911327 C>A maps to NM_007256.4 C553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr20:61291850 C>T maps to NM_016354.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1425-01A-02W-0553-09 chr8:70585478 A>G maps to NM_030958.2 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr5:101755549 C>T maps to NM_173488.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr17:33679890 T>A maps to NM_152270.3 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr17:33738674 A>G maps to NM_018042.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr17:33806778 C>T maps to ENST00000361112 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr17:33769263 T>A maps to NM_144682.5 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr17:33770903 G>A maps to NM_144682.5 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr10:98816964 A>C did not map to a codon.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr10:98823971 G>A maps to NM_003061.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr4:20619223 G>A maps to ENST00000273739 Q1446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr5:168111061 C>A maps to NM_003062.2 G1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1026-01B-01W-0484-10 chr13:84455108 G>T maps to NM_052910.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr23:144904346 G>A did not map to a codon.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr23:144905176 G>A did not map to a codon.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr23:144904006 C>T did not map to a codon.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr23:144905478 A>C did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr3:164908336 G>T maps to NM_014926.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr3:164905716 C>A maps to NM_014926.2 E968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr23:142717781 C>T did not map to a codon.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr23:142717104 A>G did not map to a codon.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr23:142718170 G>T did not map to a codon.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr23:142718595 T>C did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr13:88330417 A>G maps to NM_015567.1 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr13:88330471 G>C maps to NM_015567.1 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr10:105768063 G>T maps to NM_014720.2 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr15:59189412 A>G maps to NM_024755.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr5:159841379 T>C maps to NM_006425.4 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr18:45394715 C>T maps to NM_001003652.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr1:40878767 G>A maps to NM_022733.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr23:128649708 G>T did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:128602867 C>G did not map to a codon.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr23:128645833 G>A did not map to a codon.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr23:128624124 G>C did not map to a codon.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr23:128630778 C>T did not map to a codon.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr9:2076320 G>A maps to NM_003070.3 Q676Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr19:11105511 C>A maps to NM_001128849.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr19:11138567 C>T maps to NM_001128849.1 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr19:11113730 C>T maps to NM_001128849.1 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr2:217311805 G>A maps to NM_014140.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr2:217332750 G>A maps to NM_014140.3 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1571-01A-01W-0615-10 chr22:24175887 G>A maps to NM_003073.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr7:150937196 C>A did not map to a codon.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr23:53432591 C>A did not map to a codon.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr23:53423415 C>T did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr23:53432458 C>T did not map to a codon.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr23:53436002 G>T did not map to a codon.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr23:53436359 G>C did not map to a codon.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr23:53409160 G>T did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr23:53432033 C>G did not map to a codon.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr23:53439957 A>G did not map to a codon.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr9:106887319 G>A maps to NM_001042550.1 Q795Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1627-01A-01W-0615-10 chr9:106875658 G>A maps to NM_001042550.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr9:72897444 A>T maps to NM_015110.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr9:72920248 A>G maps to NM_015110.3 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr2:17889968 A>G maps to ENST00000381272 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr1:156233314 G>A maps to NM_015327.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr1:156230370 T>C maps to NM_015327.2 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr17:2203199 G>A maps to NM_017575.4 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr17:2203199 G>A maps to NM_017575.4 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr1:183506327 A>G maps to ENST00000367537 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr7:128846005 G>T maps to NM_005631.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr6:168927044 C>G maps to NM_022138.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr1:28280901 G>T maps to NM_014474.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr1:28282472 C>T maps to NM_014474.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr23:21995349 T>C did not map to a codon.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr11:57310463 G>T maps to ENST00000457912 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr9:33076579 C>T did not map to a codon.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr9:33068869 G>A maps to NM_018225.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr7:98636020 C>A maps to NM_020429.2 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr2:88383882 C>G maps to NM_198274.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1105-01A-01W-0484-10 chr1:214491480 A>G maps to NM_020197.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr8:49831545 C>A maps to NM_003068.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr1:227947171 C>G maps to NM_053052.3 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr6:84270651 A>T maps to NM_014841.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr5:121786272 A>G maps to ENST00000379533 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr7:127727066 G>C maps to NM_014390.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr7:127347631 G>A maps to NM_014390.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr20:1285809 G>A maps to ENST00000381876 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr20:1277866 C>G maps to ENST00000381876 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr3:43389238 C>T maps to NM_017719.4 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr2:96957180 G>T maps to NM_014014.3 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr1:31764788 C>T maps to ENST00000446633 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr20:2448389 G>A maps to ENST00000339610 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr22:24953653 T>C maps to NM_004175.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr8:51449314 C>T maps to NM_018967.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr8:51705268 C>A maps to NM_018967.2 C478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr8:51449244 T>A maps to NM_018967.2 L186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr8:51351159 G>T did not map to a codon.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr3:63649707 C>A maps to NM_001080537.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr23:70282709 A>G did not map to a codon.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr11:64799919 G>T maps to NM_013306.4 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr2:27598393 C>T maps to NM_014748.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr5:122154676 G>T maps to NM_003100.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr4:186267689 G>A did not map to a codon.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr15:75942729 G>A maps to NM_153271.1 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr3:125195601 T>A did not map to a codon.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr7:2304006 G>T maps to NM_013321.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr2:46986358 G>A maps to NM_144949.2 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr21:34922364 G>T maps to NM_138927.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr10:97096844 T>A maps to NM_001034954.1 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr4:186544514 T>A maps to ENST00000355634 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr10:108427488 G>C maps to NM_001013031.1 S754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr10:107022238 G>A maps to NM_014978.1 T1198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr10:106602581 C>T maps to NM_014978.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr10:106982967 G>T maps to NM_014978.1 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr10:106675691 T>C did not map to a codon.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr11:121461797 C>T maps to NM_003105.5 D1434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr11:121414434 G>T maps to NM_003105.5 G622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr11:121429446 T>C maps to NM_003105.5 D937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr11:121428090 T>C maps to NM_003105.5 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr1:109870142 G>A maps to NM_002959.4 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr2:39213012 G>C maps to NM_005633.3 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr14:50585460 C>A maps to NM_006939.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr13:112721998 C>T maps to NM_005986.2 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr5:157053431 C>T maps to NM_178424.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr11:16340157 T>G maps to NM_001145819.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr12:53800432 A>T maps to NM_138473.2 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr2:231406645 T>C maps to NM_001080391.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr2:231368938 C>T maps to NM_001080391.1 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr2:231331928 G>A maps to NM_001080391.1 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr2:231036819 T>A maps to NM_080424.2 K593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr2:231149124 T>C maps to NM_007237.4 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr2:231175499 G>C maps to NM_007237.4 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1728-01A-01W-0699-08 chr2:174820591 G>A maps to NM_003111.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr7:21521626 C>T maps to NM_003112.3 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr8:101237453 C>A maps to NM_003114.3 S581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr8:101253166 C>T maps to NM_003114.3 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0982-01A-01W-0488-09 chr2:214228855 T>C maps to NM_024532.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr2:214794701 T>C maps to NM_024532.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr1:118506475 T>C maps to NM_206996.2 T2206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr17:26912140 C>A maps to NM_006461.3 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr10:22676765 A>T maps to ENST00000376603 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr7:123599953 C>T maps to NM_001174046.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr23:144337310 C>A did not map to a codon.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:142795576 A>C did not map to a codon.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr23:142795566 G>T did not map to a codon.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr23:142596798 A>T did not map to a codon.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr23:142596668 G>C did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr3:172643202 C>A maps to NM_031955.5 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:217955520 C>A maps to NM_138796.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr4:52938301 G>A maps to NM_145263.2 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr4:52936031 G>C maps to NM_145263.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr1:16736124 G>A maps to NM_198546.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr15:45713329 G>A maps to NM_024063.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr15:45713251 G>T maps to NM_024063.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr14:88883124 T>G maps to NM_018418.4 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr14:88904579 G>C maps to NM_018418.4 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr8:145095089 C>T maps to NM_198572.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr6:34512223 G>A maps to NM_012391.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr11:64940669 G>T maps to NM_001008778.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr7:44046935 G>C maps to NM_175064.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr1:16261281 G>A maps to NM_015001.2 Q2849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr1:16260336 G>C maps to NM_015001.2 L2534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr1:16261173 G>C maps to NM_015001.2 G2813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr15:44912463 G>A maps to NM_025137.3 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr15:44952717 A>G maps to NM_025137.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr15:44952734 G>A maps to NM_025137.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr15:44876153 G>A maps to NM_025137.3 V1908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr16:89620250 G>A maps to NM_003119.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr2:228883301 C>T maps to NM_001142644.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr2:228881408 C>T maps to NM_001142644.1 L1387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr2:228886427 G>A maps to NM_001142644.1 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr23:57021237 T>G did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:57020871 G>A did not map to a codon.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr23:62570403 C>A did not map to a codon.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr5:147593480 T>C maps to NM_205841.3 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr19:38774399 C>T maps to NM_021102.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr1:32256845 C>T maps to NM_144569.4 E1003E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr4:167656169 C>A maps to NM_016950.2 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr17:47684703 C>A maps to NM_003563.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr15:51032025 C>T did not map to a codon.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr2:73118555 A>T maps to NM_003124.4 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr15:38643267 C>G maps to NM_152594.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr1:153004925 C>T maps to NM_003125.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr1:153066107 C>T maps to NM_001024209.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr23:155003961 C>A did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr1:158583524 A>C maps to NM_003126.2 A2325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr1:158614177 C>T maps to NM_003126.2 Q1401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr14:65261221 G>C maps to ENST00000389723 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr14:65249226 C>A maps to ENST00000389723 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr14:65237748 C>T maps to ENST00000389723 A1888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr2:54870201 T>A maps to NM_003128.2 L1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr2:54874341 C>T maps to NM_003128.2 T1647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr11:66457567 C>A maps to NM_006946.2 E1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr19:41072243 C>T maps to NM_020971.2 S2105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr19:41003431 C>T maps to NM_020971.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr19:41081354 G>C maps to NM_020971.2 S2525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr19:41007826 G>C did not map to a codon.
Sequencing variant TCGA-09-2051-01A-01W-0799-08 chr9:94821590 C>T did not map to a codon.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr14:77987879 T>G maps to NM_004863.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr8:126011653 T>A maps to NM_003129.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr5:179251005 G>A maps to NM_003900.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr20:36022357 C>T maps to ENST00000373558 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr16:30731634 C>G maps to NM_006662.2 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr22:42269824 C>G maps to NM_004599.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr16:4254546 G>A maps to ENST00000330063 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr14:35492182 A>G maps to NM_003136.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr4:57354130 A>C maps to NM_006947.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1109-01A-01W-0484-10 chr23:99921807 C>T did not map to a codon.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:99925847 T>A did not map to a codon.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr1:24989266 C>T maps to NM_005839.3 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr7:100482599 C>T maps to NM_015908.5 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr20:633634 G>C maps to NM_080725.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr19:18542825 C>T maps to NM_032627.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr11:67074400 G>A maps to NM_017857.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1673-01A-01W-0633-09 chr7:149518040 C>T maps to NM_198455.2 A4132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr7:149518040 C>T maps to NM_198455.2 A4132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr11:57095887 G>A maps to NM_003146.2 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr11:57093898 C>T maps to NM_003146.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr22:37603371 A>G maps to NM_001051.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr1:85128151 A>G maps to NM_001166417.1 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:52674513 G>T did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr8:53030926 C>A maps to NM_014682.2 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr8:53028905 G>A maps to NM_014682.2 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr3:98489734 G>T maps to ENST00000493584 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr3:186760529 C>T maps to NM_003032.2 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr3:186761000 C>G maps to NM_003032.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr2:107460241 G>A maps to NM_001142351.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr1:76877829 A>G maps to NM_152996.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr3:52551009 C>T maps to NM_015136.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr3:52555461 T>C maps to NM_015136.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr3:52548845 G>T did not map to a codon.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr12:104129310 C>T maps to NM_017564.9 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr12:104118856 C>T maps to NM_017564.9 R1596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr12:104056739 C>G maps to NM_017564.9 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr12:104131482 C>T maps to NM_017564.9 A1874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr12:104031810 C>T maps to NM_017564.9 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr12:104136181 G>C did not map to a codon.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr12:103984797 C>T maps to NM_017564.9 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1487-01A-01D-0472-08 chr3:36534719 C>T maps to NM_003149.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr23:123179100 C>T did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr23:123184054 C>A did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:123200089 A>T did not map to a codon.
Sequencing variant TCGA-25-1635-01A-01W-0615-10 chr23:123220409 G>T did not map to a codon.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr7:99796175 C>A maps to NM_012447.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr7:99798486 C>T maps to NM_012447.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr7:99779728 T>C maps to NM_012447.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr10:17746993 C>T maps to NM_003473.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr2:74058186 G>T did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr8:38002754 G>C maps to NM_000349.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr13:33739487 T>A maps to NM_178007.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr15:81605704 G>T maps to NM_181900.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr23:67937887 G>A did not map to a codon.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr23:67938363 C>A did not map to a codon.
Sequencing variant TCGA-13-1494-01A-01W-0545-08 chr23:67937369 G>A did not map to a codon.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr23:67937449 A>T did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:67943668 G>A did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:67941446 A>T did not map to a codon.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr12:57502040 G>A maps to NM_003153.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr7:89791229 C>T maps to ENST00000433102 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr11:63961671 A>G maps to ENST00000358794 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr11:63962066 C>T maps to ENST00000358794 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr5:171520430 G>T maps to NM_005990.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr2:220462834 C>A maps to NM_052902.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr7:23794027 G>T maps to NM_031414.3 G410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0714-01A-01W-0370-10 chr10:134039034 G>C maps to NM_173575.2 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr11:8414131 C>T maps to NM_030906.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1950-01A-01W-0699-08 chr6:36466138 C>T did not map to a codon.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr1:36814313 G>A maps to ENST00000373130 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr20:62273469 C>T maps to NM_015894.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr4:184932024 A>C maps to NM_020225.1 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr14:31424862 C>T maps to NM_001083893.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr14:31416426 T>C maps to NM_001083893.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr23:7268185 G>A did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr23:7268261 A>G did not map to a codon.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr1:28099859 C>T maps to ENST00000373939 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr20:57251254 C>T maps to NM_001001433.1 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr20:57246350 C>T maps to NM_001001433.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1552-01A-01W-0551-08 chr11:62595063 G>A maps to NM_003164.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr11:62592558 G>A maps to NM_003164.3 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr9:130423444 G>T maps to NM_003165.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:109321978 G>C maps to NM_007269.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr1:109315284 A>T did not map to a codon.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr1:109301202 C>T maps to NM_007269.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr3:120764380 C>T maps to NM_014980.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr3:120628436 T>C maps to NM_014980.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr2:84686348 G>A maps to NM_003849.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr3:151599176 T>G maps to NM_033050.4 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr8:70551055 T>C maps to NM_001128206.1 Y838Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr20:46294690 G>A maps to NM_001161841.1 Y604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr4:70713414 C>T did not map to a codon.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr21:46233959 G>T maps to ENST00000411651 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr20:31590697 G>A maps to NM_080675.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr6:44971494 T>C maps to NM_181356.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr19:39944004 G>T maps to NM_003169.3 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2088-01A-01W-0722-08 chr17:27005897 T>G maps to NM_003170.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr2:27880481 G>C maps to NM_014860.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2044-01B-01W-0799-08 chr9:136199560 C>T maps to NM_006753.4 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr22:24583176 C>T maps to NM_019601.3 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr1:223465979 A>G maps to NM_017982.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr3:33255451 G>A maps to NM_015551.1 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr1:149884906 G>A maps to NM_014849.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr1:149881105 C>A maps to NM_014849.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr1:149881352 T>G maps to NM_014849.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr15:91769918 G>C maps to NM_014848.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr15:91801657 C>T maps to NM_014848.4 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr15:91832844 G>C maps to NM_014848.4 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr9:113169062 T>G maps to ENST00000374463 A2942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr9:113169815 T>C maps to ENST00000374463 G2691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr9:113170322 G>A maps to ENST00000374463 T2522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr10:29777599 G>C maps to NM_021738.2 V1426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr20:58455356 C>T did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr20:58441388 T>A maps to NM_014258.2 K1427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr19:15222224 G>A maps to NM_033025.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr19:46338387 C>T maps to NM_004819.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr19:46351106 G>A maps to NM_004819.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:47433448 G>A did not map to a codon.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr23:47435600 T>C did not map to a codon.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr3:12211351 G>T maps to NM_133625.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr22:32909768 G>A maps to NM_003490.3 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr1:33160498 C>T maps to NM_030786.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr6:86324761 A>C maps to NM_006372.4 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr6:152639314 G>T maps to NM_182961.2 G5491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr6:152683378 C>A maps to NM_182961.2 E3409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr6:152777149 C>T maps to NM_182961.2 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr14:64680985 T>G maps to NM_182914.2 S6377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr14:64457274 A>G maps to NM_182914.2 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr14:64416694 T>A maps to NM_182914.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1111-01A-01W-0639-09 chr14:64428309 C>T maps to NM_182914.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr14:64596540 C>T maps to NM_182914.2 S4687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr14:64457202 A>G maps to NM_182914.2 Q796Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1336-01A-01W-0488-09 chr6:33410705 A>T maps to NM_006772.2 K793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr6:33400019 C>T maps to NM_006772.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr21:34011220 C>T maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr21:34058110 G>C maps to NM_003895.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr6:158502242 C>T maps to NM_003898.3 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr15:99672482 A>G maps to ENST00000336292 T1305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr15:99669767 G>A maps to ENST00000336292 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr15:99653863 C>T maps to ENST00000336292 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr4:119948252 G>A maps to NM_133477.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr17:35902380 G>A maps to NM_007247.4 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:49054267 C>T did not map to a codon.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr23:49049788 C>G did not map to a codon.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr1:110019430 C>T maps to NM_001040709.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr1:110018216 C>T maps to NM_001040709.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr1:110019487 C>T maps to NM_001040709.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr12:79679630 T>C maps to NM_005639.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr12:33579431 T>C did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr12:33579106 G>A maps to NM_198992.3 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr16:19194848 G>T did not map to a codon.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr1:202568417 G>T maps to NM_177402.4 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr1:114680338 G>A maps to ENST00000369545 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr11:61291332 C>G maps to NM_004200.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr11:1858459 G>T maps to NM_138567.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr11:7439230 G>T maps to NM_175733.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr11:7441835 G>A maps to NM_175733.3 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr11:85436341 C>T maps to ENST00000359152 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr11:85435366 A>T maps to ENST00000359152 T1235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr11:85435246 G>A maps to ENST00000359152 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr11:85459431 G>A maps to NM_001162953.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:99941008 T>A did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:99942146 C>G did not map to a codon.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr23:99931046 G>T did not map to a codon.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr11:64899000 G>A maps to NM_172230.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr6:132938804 G>A maps to NM_001033080.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr6:132873947 C>T maps to NM_053278.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:30873226 C>T did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:30873556 G>T did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr10:123842314 G>A maps to NM_206862.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr4:104510898 A>T maps to NM_001059.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr4:7056624 C>T maps to NM_152293.2 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr23:70602946 G>A did not map to a codon.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr23:70627867 C>G did not map to a codon.
Sequencing variant TCGA-13-0900-01B-01W-0490-10 chr23:70679489 T>G did not map to a codon.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr23:70679538 A>C did not map to a codon.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr23:70608603 G>A did not map to a codon.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr23:70614010 A>C did not map to a codon.
Sequencing variant TCGA-24-1546-01A-01W-0615-10 chr23:70601606 C>G did not map to a codon.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr9:32634323 G>A maps to NM_153809.2 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr9:32633771 G>T maps to NM_153809.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2281-01A-01W-0799-08 chr10:105147826 T>C maps to NM_006951.3 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr6:42045276 C>T maps to NM_138572.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr2:160035143 G>A maps to NM_033394.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr2:160086188 A>T maps to NM_033394.2 K1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr2:160086599 C>T maps to NM_033394.2 Q1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr17:61482568 C>T maps to ENST00000389520 R1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr17:27794197 C>T maps to NM_020791.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr16:29994520 C>T maps to NM_016151.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr12:118590130 G>A maps to NM_016281.3 Y812Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr6:32803462 G>T maps to ENST00000452392 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:234553940 A>G maps to NM_005646.3 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr1:234565354 C>T maps to NM_005646.3 W893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr1:234584272 C>T maps to NM_005646.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr1:11082198 G>T maps to NM_007375.3 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr1:11074008 C>G maps to NM_007375.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr1:19181468 G>A maps to NM_152232.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr1:19186052 G>T maps to NM_152232.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr5:9629600 C>A maps to NM_019599.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr7:141673168 G>A maps to NM_176817.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr7:142919713 G>A maps to NM_176882.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr7:143175873 C>T maps to NM_176883.2 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr12:10954679 T>G maps to NM_023919.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr12:10962143 A>G maps to NM_023917.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr4:37904124 C>T maps to NM_015173.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr4:6995909 G>C did not map to a codon.
Sequencing variant TCGA-29-1697-01A-01W-0633-09 chr4:26721733 T>C maps to NM_018317.2 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1328-01A-01W-0492-08 chr23:48417293 T>C did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr17:18541682 C>T maps to NM_001039397.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0751-01A-01D-0446-08 chr13:75869116 A>G maps to ENST00000431480 H1064H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr23:106064216 A>G did not map to a codon.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr23:106070471 C>T did not map to a codon.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr23:106113968 G>C did not map to a codon.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr23:106111652 C>A did not map to a codon.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr5:179334814 G>A maps to NM_198868.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:9673063 C>A did not map to a codon.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr2:162273382 C>T maps to NM_006593.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr6:85472350 C>T maps to NM_001080508.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr17:59480474 C>T maps to NM_005994.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr23:79281243 C>A did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr23:79286131 C>A did not map to a codon.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr12:115117723 A>G maps to NM_016569.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1648-01A-01W-0639-09 chr12:114793708 G>A maps to NM_000192.3 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr12:114793777 C>T maps to NM_000192.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr12:114793543 C>T maps to NM_000192.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr14:92253872 T>G maps to NM_001128596.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr23:102884960 G>A did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr23:102885157 G>A did not map to a codon.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr23:102841739 A>C did not map to a codon.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr23:101396191 C>T did not map to a codon.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr23:102508778 G>A did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr23:13680752 T>C did not map to a codon.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr18:44560048 C>T maps to NM_016427.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr5:145849167 A>G maps to NM_006706.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr10:133106528 C>T maps to NM_174937.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr15:57574748 G>C maps to NM_207036.1 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr15:57545611 C>A maps to NM_207036.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr15:57554347 T>C maps to NM_207036.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr22:42608131 G>C maps to NM_005650.1 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr22:42609745 G>C maps to NM_005650.1 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr18:52895487 C>A maps to ENST00000398339 G764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr1:152084051 C>T maps to NM_007113.2 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr11:67815136 C>A maps to NM_006019.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr14:96178658 G>T maps to NM_021966.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr14:96157185 C>T maps to NM_004918.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr5:149753734 A>C did not map to a codon.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr12:106704900 C>T maps to NM_152772.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr12:106715292 C>T maps to NM_152772.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2260-01A-01W-0722-08 chr12:124179491 T>A maps to NM_024809.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr3:46621295 C>A maps to NM_003212.3 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr10:115980602 G>T did not map to a codon.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr1:179609180 C>T maps to ENST00000444136 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr6:46658990 C>G maps to NM_001010870.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0723-01A-02W-0372-09 chr9:100237742 C>T maps to NM_014290.2 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr14:104482382 G>T maps to NM_153046.2 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr14:104457533 C>T maps to NM_153046.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr1:151755384 C>T maps to NM_001083965.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr19:49860523 G>T maps to NM_003598.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr11:121028626 G>A maps to NM_005422.2 P1461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr11:120984335 C>A maps to NM_005422.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr2:95539775 C>A maps to NM_144705.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr2:95537690 A>T maps to NM_144705.2 K123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr16:10721463 G>A maps to NM_144674.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr14:20836604 A>G maps to NM_007110.4 N2625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr14:20851454 G>A maps to NM_007110.4 Q1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr14:20864063 G>A maps to NM_007110.4 N568N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr8:73937055 G>A did not map to a codon.
Sequencing variant TCGA-23-2643-01A-01D-1526-09 chr7:115889145 A>G maps to NM_015641.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr1:45810772 G>C maps to NM_007170.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr10:70406106 T>G maps to NM_030625.2 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr10:70442636 G>A maps to NM_030625.2 K1653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr9:103108398 G>A maps to NM_017746.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr19:43920392 A>T maps to NM_031451.4 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1665-01B-01W-0615-10 chr23:69826841 C>T did not map to a codon.
Sequencing variant TCGA-10-0926-01A-01W-0420-08 chr23:69826839 A>G did not map to a codon.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr23:69945169 A>G did not map to a codon.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr23:104464291 C>G did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:104464722 G>A did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:104464792 C>T did not map to a codon.
Sequencing variant TCGA-61-1995-01A-01W-0722-08 chr23:104464851 C>T did not map to a codon.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr23:107225183 C>A did not map to a codon.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr17:56661917 A>G maps to ENST00000240361 H1044H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr17:62265563 C>G maps to NM_018469.3 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr3:51718562 G>A maps to NM_015926.4 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr6:50718992 T>C maps to NM_172238.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr2:121992810 G>A maps to NM_014553.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr13:114288851 G>T maps to NM_007111.4 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr13:114288335 T>C maps to NM_007111.4 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0975-01B-02W-0486-08 chr23:132351860 C>G did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr23:48891026 G>A did not map to a codon.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr6:41655673 C>G maps to ENST00000343317 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr22:26892054 G>A maps to NM_012143.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr7:100224454 C>T maps to NM_003227.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr7:100225099 G>T maps to NM_003227.3 Y594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr3:195779028 G>A maps to NM_001128148.1 Y689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr3:195785485 A>C maps to NM_001128148.1 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr8:134042139 C>T maps to NM_003235.4 R2371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr8:133925441 G>A maps to NM_003235.4 W1437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr8:133900727 T>C maps to NM_003235.4 H892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr8:134024173 C>T maps to NM_003235.4 A2097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr8:133885424 C>T maps to NM_003235.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1764-01A-01W-0633-09 chr8:133900277 G>A maps to NM_003235.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2350-01A-01W-0799-08 chr5:135389656 A>C maps to NM_000358.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr9:101900288 G>T maps to NM_004612.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr1:92185569 G>A maps to NM_003243.4 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr23:89177101 C>T did not map to a codon.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr20:36779361 G>A maps to NM_004613.2 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr20:36758623 G>A maps to NM_004613.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr3:44952865 G>T maps to NM_003241.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr20:2397926 C>T maps to NM_198994.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr20:2398127 C>G maps to NM_198994.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr20:2380979 G>T maps to NM_198994.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr20:2380265 C>T maps to NM_198994.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1995-01A-01W-0722-08 chr15:43571404 G>A maps to NM_052955.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr15:43579830 G>A maps to NM_052955.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr2:43520302 T>A maps to ENST00000330266 G1497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr2:43514122 T>C maps to ENST00000330266 T1697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr15:71174912 T>C maps to NM_020147.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0968-01A-01W-0484-10 chr2:242545727 C>T did not map to a codon.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr4:83838348 T>C maps to NM_024672.4 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr15:39876541 T>A maps to NM_003246.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr15:39886352 C>T maps to NM_003246.2 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2409-01A-01W-0799-08 chr6:169650826 C>T did not map to a codon.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr6:169625423 G>A maps to NM_003247.2 D863D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr19:362214 G>A maps to NM_016585.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr1:151823622 C>A maps to NM_182578.3 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr1:151824770 C>A maps to NM_182578.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr6:128134405 C>T maps to NM_001164685.1 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr2:88485423 C>A maps to NM_018271.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr23:122829903 C>T did not map to a codon.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr23:122866860 C>T did not map to a codon.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr23:122760387 G>T did not map to a codon.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr23:122759895 G>C did not map to a codon.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr23:122771929 T>A did not map to a codon.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr23:122800994 G>C did not map to a codon.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr17:38244742 A>G maps to NM_003250.5 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr1:36762272 T>A maps to NM_005119.3 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr13:52971790 A>T maps to NM_018676.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0366-01A-01W-0372-09 chr7:11675820 G>A maps to ENST00000423059 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr7:11676208 A>C maps to ENST00000423059 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0975-01B-02W-0486-08 chr7:11419268 C>G maps to ENST00000423059 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr3:9412892 T>C maps to NM_015453.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr6:155566794 C>T maps to ENST00000456144 Y1194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr6:155458321 C>A maps to ENST00000456144 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr1:43786954 C>A maps to NM_005424.2 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr4:153691679 C>T maps to NM_145720.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr5:149374597 G>A maps to NM_030953.2 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr5:156378556 G>A maps to NM_138379.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr12:56815920 C>T maps to NM_003920.3 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1510-01A-02D-0472-08 chr12:56824744 G>T maps to NM_003920.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr12:56817081 A>G maps to NM_003920.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr12:56817374 G>A maps to NM_003920.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr23:48751254 C>G did not map to a codon.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr19:39978810 C>G maps to NM_001001563.1 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr19:39971489 C>G maps to NM_001001563.1 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1353-01A-01D-1526-09 chr6:54214690 C>A maps to NM_014464.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr3:156421398 C>T maps to NM_015508.4 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr3:156395503 C>T maps to NM_015508.4 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1575-01A-01W-0615-10 chr1:168165879 G>A maps to NM_152902.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr15:30025329 C>T maps to NM_003257.3 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr19:3735865 G>T did not map to a codon.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr19:3740718 C>T maps to NM_014428.1 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr23:153543600 G>A did not map to a codon.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr23:153549203 G>C did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr23:153541112 G>T did not map to a codon.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr23:153524339 G>A did not map to a codon.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr9:82319727 C>T maps to ENST00000376537 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr4:166916240 C>T maps to ENST00000507499 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr9:35724623 C>A maps to NM_006289.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2045-01A-01W-0799-08 chr15:63112742 G>A maps to NM_015059.2 G2312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr15:63131053 G>A did not map to a codon.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr15:63029164 C>T maps to NM_015059.2 A1149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr15:62948200 G>A maps to NM_015059.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr9:120476760 G>C maps to NM_138554.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr1:223286049 G>T maps to NM_003268.5 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr1:223284969 G>T maps to NM_003268.5 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr23:12905366 T>C did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:12903900 G>A did not map to a codon.
Sequencing variant TCGA-25-1635-01A-01W-0615-10 chr23:12904345 T>C did not map to a codon.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr23:12938694 G>T did not map to a codon.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr23:12938880 A>T did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr23:12938968 A>T did not map to a codon.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr23:12939055 T>A did not map to a codon.
Sequencing variant TCGA-36-2540-01A-01D-1526-09 chr23:12937754 C>T did not map to a codon.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr23:12938669 T>A did not map to a codon.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr1:62190762 A>C maps to ENST00000371180 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr1:62174998 A>C did not map to a codon.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr3:149093267 G>A maps to ENST00000383054 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr17:4685820 G>A maps to NM_003963.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr13:100181836 T>C maps to NM_004800.1 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr12:66546128 G>A maps to ENST00000286424 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr9:75435907 C>T maps to NM_138691.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr20:2592922 C>A maps to NM_080751.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr16:68894360 C>T maps to NM_024562.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr19:10945963 G>T maps to NM_006858.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr1:93645703 G>C maps to NM_016040.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr16:69377330 A>G maps to NM_144676.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr14:77809608 G>C maps to NM_213601.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr17:79287663 G>T maps to NM_178520.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr12:44781917 G>A maps to NM_032256.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr12:108986030 C>T maps to NM_181724.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr12:108985583 G>A maps to NM_181724.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr12:122199614 G>A maps to NM_001080825.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr7:98460785 C>T maps to NM_001134450.1 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1632-01A-01W-0615-10 chr7:98452933 G>T maps to NM_001134450.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr7:98445825 C>T maps to NM_001134450.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1580-01A-01W-0615-10 chr7:98446204 C>A did not map to a codon.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr2:98413915 G>A maps to NM_015348.1 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr2:98392470 T>C maps to NM_015348.1 K1385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1506-01A-01W-0549-09 chr12:126135438 C>T maps to NM_052907.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr12:126135285 C>T maps to NM_052907.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr12:126138277 A>G maps to NM_052907.2 E753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr12:129558862 C>A maps to NM_133448.2 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr12:129566555 C>T maps to NM_133448.2 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr12:130184521 G>A maps to NM_133448.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr12:129563123 G>T maps to NM_133448.2 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr12:129559048 G>A maps to NM_133448.2 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr12:130185031 G>A maps to NM_133448.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr17:32964656 C>T maps to NM_207313.1 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr11:120198133 G>A maps to NM_001198670.1 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr4:153601073 G>C maps to NM_152680.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr4:122681607 G>A maps to NM_152399.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr16:21190855 C>T maps to ENST00000451578 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr19:19243234 G>C maps to NM_017814.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr7:112407692 A>C maps to NM_022484.4 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr2:120438939 C>T maps to NM_030577.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr2:103380881 A>C maps to NM_144632.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr23:148690458 A>T did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr12:57472510 T>C maps to NM_001130963.1 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr9:74305102 C>T maps to NM_013390.2 P1252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr9:74365244 T>C maps to NM_013390.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1664-01A-01W-0639-09 chr1:27661929 C>T maps to NM_032125.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr23:15646101 G>A did not map to a codon.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr3:119151001 G>A maps to NM_018266.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2588-01A-01D-1526-09 chr3:100274160 C>A maps to ENST00000403410 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr21:34828044 A>C maps to NM_006134.5 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr1:45120308 G>A maps to NM_024587.2 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1725-01A-01W-0639-09 chr8:92008042 G>T maps to NM_018710.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr7:77423645 G>A maps to NM_032936.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr15:43438758 C>A maps to NM_024956.3 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr1:226034784 G>A maps to NM_014698.2 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr14:77705772 T>C maps to NM_020431.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr8:94809682 C>T maps to NM_153704.5 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr8:133740206 C>G maps to ENST00000395406 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr8:133764200 G>A maps to ENST00000395406 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr15:42529627 A>T did not map to a codon.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr3:48658922 C>A maps to NM_001008269.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr23:154754254 C>T did not map to a codon.
Sequencing variant TCGA-25-1627-01A-01W-0615-10 chr12:98941440 T>C maps to NM_001032283.2 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr12:98927520 G>T maps to NM_003276.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1625-01A-01W-0615-10 chr4:69096979 G>T maps to NM_182502.3 Y209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr4:68964725 T>A maps to NM_207407.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr4:68938038 A>C did not map to a codon.
Sequencing variant TCGA-30-1853-01A-02W-0699-08 chr21:43795839 G>A maps to ENST00000380399 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr12:88586467 T>C maps to NM_181783.3 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr13:101264687 C>G maps to NM_032813.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr13:101287145 C>T maps to NM_032813.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr18:66381129 T>A maps to NM_019022.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr8:23049491 G>T maps to NM_003844.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr12:6438477 T>A maps to NM_001065.3 *456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr1:12164532 T>C maps to NM_001243.3 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr1:12175721 C>A maps to NM_001243.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr1:12144523 C>T maps to NM_001243.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr1:173155804 A>G maps to NM_003326.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr5:150441738 G>C maps to NM_006058.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr4:122068295 G>A maps to ENST00000509841 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr3:195611841 C>T maps to NM_001010938.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr3:195615447 C>T maps to NM_001010938.1 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr1:175066670 C>T maps to NM_022093.1 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr1:74905202 C>T maps to NM_001112808.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr1:74957818 C>T maps to NM_001112808.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr7:128655106 G>T maps to ENST00000471166 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr7:128612518 C>T maps to ENST00000471166 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr7:128640521 C>T maps to ENST00000471166 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr1:175372582 G>A maps to NM_003285.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr1:175328793 T>A maps to NM_003285.2 P976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr16:24817969 C>T maps to NM_014494.2 Q1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr16:24817559 C>T maps to NM_014494.2 Q1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr2:218682899 G>A maps to NM_022648.4 G1281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr7:47342860 T>A maps to NM_022748.11 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr7:47451347 G>A maps to NM_022748.11 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr6:32047023 C>T maps to ENST00000375244 S1387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr6:32012918 G>A maps to ENST00000375244 P3597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr6:31979011 C>T maps to NM_032470.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr22:41832899 C>G maps to NM_016272.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr1:45808945 C>T maps to NM_025077.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr19:45397255 G>C maps to NM_006114.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr17:38567938 G>C maps to ENST00000357601 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr9:32542100 C>A maps to NM_005802.4 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr1:179820118 G>C maps to NM_145034.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr1:179057053 G>A maps to NM_022371.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-04-1365-01A-01W-0490-10 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-04-1516-01A-01D-1526-09 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1517-01A-01W-0615-10 chr17:7579493 T>A maps to NM_001126112.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1659-01B-01W-0615-10 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-09-1666-01A-01W-0615-10 chr17:7578554 C>A did not map to a codon.
Sequencing variant TCGA-09-1669-01A-01W-0615-10 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr17:7578289 C>G did not map to a codon.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0884-01B-01W-0494-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr17:7578554 C>A did not map to a codon.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr17:7579388 G>A maps to NM_001126112.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr17:7578368 A>C did not map to a codon.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr17:7577497 C>A did not map to a codon.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr17:7574033 C>T did not map to a codon.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-23-1107-01A-01W-0484-10 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr17:7577578 G>C maps to NM_001126112.1 Y234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0970-01B-01W-0486-08 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr17:7577017 C>T did not map to a codon.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr17:7576851 C>G did not map to a codon.
Sequencing variant TCGA-24-1471-01A-01W-0551-08 chr17:7577126 C>A maps to NM_001126112.1 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr17:7576926 C>T did not map to a codon.
Sequencing variant TCGA-24-1557-01A-01W-0615-10 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr17:7579591 T>A did not map to a codon.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr17:7576926 C>T did not map to a codon.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr17:7573981 C>A maps to NM_001126112.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr17:7579527 C>T maps to NM_001126112.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr17:7576884 T>A maps to NM_001126112.1 K321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2289-01A-01W-0799-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr17:7579535 C>A maps to NM_001126112.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1631-01A-01W-0615-10 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr17:7574034 T>C did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-29-1785-01A-01W-0633-09 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-36-1569-01A-01W-0615-10 chr17:7579528 C>T maps to NM_001126112.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2355-01A-01W-0799-08 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr17:7577024 T>A maps to NM_001126112.1 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2016-01A-01W-0722-08 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2003-01A-01W-0722-08 chr1:223986085 G>A maps to NM_001031685.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr11:44956511 G>A maps to NM_006034.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr20:44006228 C>A maps to NM_014477.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1655-01A-01W-0633-09 chr6:83075391 C>T maps to NM_006670.4 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr11:68822260 C>T maps to NM_139075.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr11:68853168 T>C maps to NM_139075.3 C623C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr20:62507183 T>A maps to NM_199360.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr12:72335392 C>T maps to ENST00000389376 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr12:6979226 C>T maps to NM_001159287.1 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr19:16178451 G>A maps to NM_001145160.1 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2409-01A-01W-0799-08 chr2:1488399 C>T maps to NM_000547.5 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr1:186328957 T>C maps to NM_003292.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2271-01A-01W-0799-08 chr1:186312597 G>A maps to NM_003292.2 R1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr1:186287709 G>A maps to NM_003292.2 T2230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr1:3545056 C>T maps to NM_182752.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr2:73961606 T>C maps to ENST00000409716 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr21:10941964 A>G maps to NM_199261.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr13:20041411 A>G maps to NM_199254.2 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2396-01A-01W-0799-08 chr6:111901530 C>T maps to ENST00000340026 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr1:211545788 G>T maps to ENST00000427925 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr2:202262942 T>C maps to NM_015049.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr8:141461132 G>T maps to NM_031466.5 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1695-01A-01W-0633-09 chr10:17199453 C>A maps to NM_004412.5 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr6:123869663 A>T maps to NM_006073.2 L109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr6:42231078 C>T maps to NM_033502.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr12:72893327 C>T maps to NM_013381.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr20:376868 G>A maps to ENST00000422053 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr6:30128542 G>A maps to NM_006778.3 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr13:50586658 C>T maps to NM_001007278.1 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr6:30131601 G>T maps to NM_033229.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr17:15535914 G>T maps to ENST00000455584 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr5:64892341 A>G maps to NM_001656.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr5:64909989 G>A maps to NM_001656.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr7:138261139 A>C maps to NM_015905.2 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr11:6478208 G>A maps to NM_033278.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr6:30071438 A>G maps to NM_007028.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr9:119460734 C>T maps to NM_012210.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr5:114469587 T>C maps to NM_018700.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr6:30309876 C>T maps to NM_021253.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr6:30297547 G>T did not map to a codon.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr6:30115573 C>G maps to ENST00000376724 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr3:140406646 G>T maps to NM_152616.4 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr17:73872051 G>A maps to NM_033452.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr11:5699664 C>T did not map to a codon.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr11:5701014 T>C maps to NM_033034.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr8:67039616 G>A maps to NM_184085.1 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr1:248039703 G>A maps to NM_015431.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1694-01A-01W-0633-09 chr1:231335998 T>C maps to NM_001004342.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr5:180627009 C>T maps to NM_203293.1 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr3:32932168 C>T maps to NM_001039111.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr4:189068430 C>T maps to NM_178556.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr5:14297203 C>G maps to NM_007118.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr5:14406747 A>G maps to NM_007118.2 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr5:14369480 A>T did not map to a codon.
Sequencing variant TCGA-13-0916-01A-01W-0420-08 chr14:92439175 T>A maps to NM_004239.3 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr14:92480574 T>C maps to NM_004239.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr2:230650511 G>A maps to ENST00000389044 G1658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1553-01A-01W-0552-10 chr5:914603 C>T maps to NM_004237.3 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr15:64690017 G>T did not map to a codon.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr6:126333933 G>T maps to NM_001031712.2 E315*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-61-1733-01A-01W-0639-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-24-1604-01A-01W-0552-10 chr23:100276967 G>A did not map to a codon.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr22:46742394 T>G maps to NM_018006.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr1:28891298 C>T maps to NM_017846.4 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr23:54950144 C>A did not map to a codon.
Sequencing variant TCGA-29-1783-01A-01W-0633-09 chr23:54952107 A>C did not map to a codon.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr8:72948575 A>G maps to NM_007332.2 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr8:72950286 A>G maps to NM_007332.2 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr8:72981272 A>G maps to NM_007332.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr8:72958747 G>A maps to NM_007332.2 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr4:122853734 G>A maps to NM_001130698.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr13:38225512 G>C maps to NM_003306.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr13:38225538 C>A maps to NM_003306.1 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr23:111078156 G>T did not map to a codon.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr15:31338415 C>T maps to NM_002420.4 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr15:31318394 C>T maps to NM_002420.4 K1170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr21:45789180 C>T maps to ENST00000397932 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr9:73477871 A>C maps to ENST00000419692 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr9:73168116 C>A maps to ENST00000419692 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr9:73233959 G>A maps to ENST00000419692 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr9:73218365 C>T maps to ENST00000419692 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr11:2432891 G>C maps to ENST00000452833 G862G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr2:234869688 C>T maps to NM_024080.4 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr17:3427613 A>G maps to ENST00000381913 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr17:3427602 G>A maps to ENST00000381913 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr17:3430170 C>T maps to ENST00000381913 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr17:3458090 G>C maps to ENST00000381913 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr7:142625187 G>T maps to NM_019841.4 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr7:142626207 G>A maps to NM_019841.4 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2016-01A-01W-0722-08 chr7:142569717 G>A maps to NM_018646.2 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr7:98573788 C>T maps to ENST00000359863 S2612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr7:98495485 A>C maps to ENST00000359863 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr7:98592277 G>T maps to ENST00000359863 V3358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr7:98553770 G>A maps to ENST00000359863 V1973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr7:98553851 C>T maps to ENST00000359863 I2000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1646-01A-01W-0639-09 chr9:135781377 G>A maps to NM_000368.4 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1603-01A-01W-0551-08 chr9:135778138 C>T maps to NM_000368.4 Q748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr9:135779828 G>T maps to NM_000368.4 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr12:58190305 G>A maps to NM_001172696.1 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr7:130368491 T>G maps to NM_052933.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1576-01A-01W-0615-10 chr14:81609346 G>C maps to NM_000369.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1576-01A-01W-0615-10 chr14:81609652 G>C maps to NM_000369.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1661-01B-01W-0615-10 chr20:51873044 G>A maps to NM_173485.5 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1346-01A-01W-0488-09 chr19:31770077 G>A maps to NM_020856.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr19:31768043 C>T maps to NM_020856.2 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1426-01A-01W-0549-09 chr1:46650756 C>T maps to NM_005727.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2392-01A-01W-0799-08 chr10:82269139 C>T maps to NM_030927.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr12:85417151 A>G maps to NM_001100917.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr4:99399946 C>G maps to NM_005723.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr23:99888434 A>C did not map to a codon.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr23:38530638 T>A did not map to a codon.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr12:3387607 G>T maps to ENST00000407263 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr6:116600320 C>A maps to NM_003309.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1577-01A-01W-0615-10 chr6:116600084 G>C maps to NM_003309.3 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr23:53115192 G>A did not map to a codon.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr8:98289379 C>G maps to NM_033512.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1768-01A-01W-0633-09 chr8:98289400 A>G maps to NM_033512.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr5:112769969 G>A maps to NM_032028.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr15:43044267 C>T maps to ENST00000263802 W1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr11:113220878 G>T maps to NM_017868.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr1:231060660 C>T maps to NM_024525.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr3:180327948 T>C maps to NM_133462.3 Y644Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr11:43511796 G>A maps to NM_018259.5 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr11:43465706 C>G maps to NM_018259.5 Y871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2081-01A-01W-0722-08 chr11:43427398 C>T maps to NM_018259.5 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr10:75107940 G>C maps to NM_145170.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr10:75107961 C>T maps to NM_145170.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr2:166770098 G>T maps to NM_024753.3 Y732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr2:166799727 C>A did not map to a codon.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr17:40095356 G>A maps to ENST00000377543 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr7:138831940 C>T maps to NM_024926.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr2:32903967 G>A maps to NM_017735.4 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr4:147628653 A>G maps to ENST00000513335 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr5:40716468 T>C maps to NM_012382.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1023-01A-03W-0484-10 chr5:40716407 C>A maps to NM_012382.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1616-01A-01W-0553-09 chr5:94857880 C>A maps to NM_014639.3 E630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr5:94805497 G>C maps to NM_014639.3 R1494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr22:46677512 G>T maps to NM_017931.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr2:47278960 C>A maps to ENST00000394850 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr14:91084325 A>T maps to NM_001010854.1 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1349-01A-01W-0494-09 chr11:62496463 G>T maps to NM_173810.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr6:80721177 C>G maps to NM_003318.4 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr6:80747706 A>C maps to NM_003318.4 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr22:43570279 G>A maps to NM_015140.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr3:9876892 C>A maps to NM_001025930.3 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2077-01A-01W-0722-08 chr14:76211897 T>A maps to NM_015072.4 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr14:76232699 T>C maps to NM_015072.4 N668N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr22:50471791 C>A maps to NM_001080447.1 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr20:30530751 C>T maps to NM_001008409.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1365-01A-01W-0490-10 chr2:179645974 G>T maps to NM_133378.4 Y1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1542-01A-01W-0553-09 chr2:179615843 C>T maps to ENST00000375038 K3763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr2:179397439 T>C maps to NM_133378.4 P32066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr2:179485026 G>A maps to NM_133378.4 D12839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr2:179613554 A>G maps to ENST00000375038 D4526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr2:179643656 A>G maps to NM_133378.4 A1384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr2:179479649 G>A maps to NM_133378.4 R13660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr2:179454987 C>A maps to NM_133378.4 V17920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr2:179465863 G>T maps to NM_133378.4 G16021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr2:179398819 G>C maps to NM_133378.4 V31606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr2:179579190 G>A maps to NM_133378.4 F7526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr2:179425004 T>G maps to NM_133378.4 G26050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr2:179584364 C>A maps to NM_133378.4 E6708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2290-01A-01W-0799-08 chr2:179628949 A>T maps to NM_133378.4 T3356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1313-01A-01W-0492-08 chr2:179612537 A>T maps to ENST00000375038 V4865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1318-01A-01W-0490-10 chr2:179399719 G>A maps to NM_133378.4 N31306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr2:179641543 G>A maps to NM_133378.4 R1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr2:179604887 C>A maps to NM_133437.3 E4187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr2:179496982 G>A maps to NM_133378.4 D11978D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr2:179436062 T>C maps to NM_133378.4 P22364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:179458949 G>T maps to NM_133378.4 L16822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr2:179615936 T>C maps to ENST00000375038 R3732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr2:179404666 T>A maps to NM_133378.4 R30141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2429-01A-01D-1526-09 chr2:179629407 C>A maps to NM_133378.4 L3278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr2:179474500 C>A maps to NM_133378.4 E14649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr2:179612114 G>A maps to ENST00000375038 D5006D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1738-01A-01W-0639-09 chr2:179438583 G>T maps to NM_133378.4 S21524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr2:179594389 C>A did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr2:179408636 G>C maps to NM_133378.4 Y29510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr2:179397415 A>T maps to NM_133378.4 P32074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr2:179654827 A>G maps to NM_133378.4 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2095-01A-01W-0722-08 chr2:179432534 C>T maps to NM_133378.4 Q23540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2614-01A-01W-1092-09 chr2:179641160 C>T maps to NM_133378.4 R1810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr17:72248452 C>T maps to NM_032646.5 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr17:72246456 C>T maps to NM_032646.5 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr17:72239608 G>C did not map to a codon.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr12:49523281 C>A did not map to a codon.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr13:19752478 G>A maps to NM_006001.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0897-01A-01W-0421-09 chr13:19751363 C>T maps to NM_006001.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr13:19751363 C>T maps to NM_006001.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr6:30691258 C>T maps to NM_178014.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1690-01A-01W-0633-09 chr6:30691285 T>A maps to NM_178014.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr4:190904328 G>T maps to ENST00000248151 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2079-01A-01W-0722-08 chr6:112397246 C>T maps to NM_016262.4 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr17:40817778 G>C maps to NM_016437.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr15:43668411 T>C maps to ENST00000399460 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr22:50658082 G>A maps to NM_020461.3 Y1435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr22:50659451 G>A maps to NM_020461.3 N1112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1730-01A-01W-0639-09 chr12:3047446 T>C maps to NM_001160408.1 N397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr6:158900799 C>A maps to NM_020245.3 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr8:15588172 A>G did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr17:6546272 T>G maps to NM_032731.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr18:9887063 G>A maps to NM_001098529.1 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr18:9887219 G>A maps to NM_001098529.1 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1418-01A-01W-0549-09 chr1:145440069 T>A maps to NM_006472.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr1:145440431 A>G maps to NM_006472.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr22:19902745 G>C maps to NM_006440.3 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr19:10464311 C>T maps to NM_003331.4 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2363-01A-01W-0799-08 chr22:50966137 C>T maps to ENST00000395681 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr11:88911741 T>C maps to NM_000372.4 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr11:89028422 A>G maps to NM_000372.4 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr15:41870119 C>G maps to NM_006293.3 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2061-01A-01D-1526-09 chr9:12694226 T>C maps to NM_000550.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr10:71899804 G>A maps to NM_173555.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr1:162535875 C>G maps to ENST00000367925 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr1:162549331 C>T maps to ENST00000367925 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:47074274 G>A did not map to a codon.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr23:47065671 C>G did not map to a codon.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr19:34949672 G>T did not map to a codon.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr21:43838667 G>A maps to NM_018961.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr2:181846834 G>T maps to NM_182678.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr4:39779300 G>C did not map to a codon.
Sequencing variant TCGA-61-1728-01A-01W-0699-08 chr11:57327835 G>A maps to NM_004223.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1501-01A-01W-0545-08 chr15:76165767 G>T did not map to a codon.
Sequencing variant TCGA-29-2431-01A-01D-1526-09 chr15:76175726 T>C maps to NM_173469.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1361-01A-01W-0494-09 chr7:157041087 G>A maps to NM_014671.2 E836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:10238757 G>C maps to NM_001105562.2 G1194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr20:3102633 C>T maps to NM_014948.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1470-01A-01W-0553-09 chr23:56591171 G>T did not map to a codon.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr6:42573530 T>C maps to NM_015255.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0717-01A-01W-0370-10 chr1:19518748 G>A maps to ENST00000375267 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:19443875 C>T maps to ENST00000375267 T3554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1548-01A-01W-0615-10 chr1:19454182 T>G maps to ENST00000375267 V3054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2432-01A-01D-1526-09 chr1:19473416 C>T maps to ENST00000375267 V2569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr8:103323724 C>T did not map to a codon.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr5:171639070 C>T maps to NM_152277.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr17:42288463 G>A maps to NM_014233.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr1:20517092 G>A maps to NM_152376.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr19:4452482 C>A maps to NM_025241.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr11:73715550 C>G maps to NM_003356.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1469-01A-01W-0553-09 chr9:114691946 G>A maps to NM_003358.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr4:39511971 C>A did not map to a codon.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr13:96579326 T>A maps to NM_020121.3 K719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr2:234591342 C>T maps to ENST00000373460 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1110-01A-01D-0428-08 chr2:234526585 C>G maps to NM_019076.4 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1332-01A-01W-0488-09 chr2:234581344 G>A maps to NM_021027.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr2:234580973 A>T maps to NM_021027.2 K132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr4:70505198 G>A maps to ENST00000514019 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr4:69693266 G>C did not map to a codon.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr4:69682126 T>C maps to NM_001075.4 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr4:69433614 A>G maps to NM_001076.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr4:70346446 G>A maps to NM_021139.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr4:69974040 G>C did not map to a codon.
Sequencing variant TCGA-13-0924-01A-01W-0421-09 chr5:35954510 C>A maps to NM_152404.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0933-01A-01W-0421-09 chr4:115544518 C>T maps to NM_003360.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr19:4944463 T>C did not map to a codon.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr6:34826115 G>C maps to NM_017754.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr5:176338310 C>T did not map to a codon.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr3:41746787 T>A maps to NM_017886.2 K882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr19:17737485 G>A maps to ENST00000428389 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr9:35377621 G>A maps to ENST00000396787 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr15:54307265 A>C maps to ENST00000260323 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1685-01A-01W-0633-09 chr15:54305270 C>A maps to ENST00000260323 Y57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr15:54435869 G>A maps to ENST00000260323 Q1020Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr15:54306222 C>T maps to ENST00000260323 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr17:33482455 C>A maps to NM_173167.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr17:33513322 C>A maps to NM_173167.2 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr17:33475449 G>A maps to NM_173167.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1707-01A-01W-0633-09 chr5:176297377 C>T maps to NM_133369.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr4:96222850 T>C maps to NM_003728.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0903-01A-01W-0421-09 chr8:35544090 A>G maps to ENST00000416672 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr12:109537067 C>G maps to NM_080911.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr17:73816189 G>C did not map to a codon.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr16:1449439 G>T maps to ENST00000508903 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr22:24909449 C>T maps to NM_016327.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr19:18963026 C>T maps to ENST00000418384 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-24-2254-01A-01W-0722-08 chr23:118975081 C>T did not map to a codon.
Sequencing variant TCGA-36-2542-01A-01D-1526-09 chr23:118972369 T>A did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr22:30163395 C>T maps to ENST00000406782 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1530-01A-02W-0552-10 chr3:48638210 G>C maps to NM_003365.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0979-01A-01W-0486-08 chr7:43917885 C>T maps to NM_001077663.1 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr1:45477951 G>T maps to NM_000374.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr11:17531981 C>T maps to NM_153676.3 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr1:215848346 C>T maps to ENST00000366943 R4302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr1:215963505 A>T maps to ENST00000366943 C3359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr1:215807953 C>T maps to ENST00000366943 A5048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr1:216040512 C>A did not map to a codon.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr1:215972432 C>A maps to ENST00000366943 R3258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr1:216420526 G>A maps to ENST00000366943 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr1:215914790 C>A maps to ENST00000366943 G3879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr1:215812578 G>T maps to ENST00000366943 T4990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr1:216420002 G>T maps to ENST00000366943 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1337-01A-01W-0484-10 chr4:76721616 C>G maps to NM_003715.2 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr23:47101534 G>A did not map to a codon.
Sequencing variant TCGA-36-1571-01A-01W-0615-10 chr23:47098491 A>G did not map to a codon.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr3:179458042 G>A maps to NM_003940.2 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1419-01A-01W-0545-08 chr3:179478936 C>G maps to NM_003940.2 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr3:179470150 C>G maps to NM_003940.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr3:49153261 C>T maps to ENST00000434032 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr3:49154035 G>A maps to ENST00000434032 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr3:49148250 C>A maps to ENST00000434032 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2111-01A-01W-0722-08 chr11:119227994 G>A maps to NM_004205.4 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr1:161132064 C>T maps to NM_012475.4 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr1:55612631 A>C maps to NM_015306.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr21:17242433 C>G maps to ENST00000285681 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2293-01A-01W-0799-08 chr21:17250185 C>T maps to ENST00000285681 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1862-01A-02W-0699-08 chr21:17199304 A>G maps to ENST00000285681 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr23:132162151 T>A did not map to a codon.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr11:113674594 C>T maps to NM_020886.2 W888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr11:113701645 C>A maps to NM_020886.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr19:57642197 A>T maps to NM_020903.2 K719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr19:57640846 A>G maps to NM_020903.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr19:57641098 G>A maps to NM_020903.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr16:23080131 C>T maps to NM_020718.3 E1098E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1776-01A-01W-0639-09 chr17:58284465 G>A maps to NM_032582.3 R985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr2:61575537 C>A maps to NM_014709.3 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr2:61522380 G>A maps to NM_014709.3 S1433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-0980-01A-01W-0421-09 chr2:61475757 A>G maps to NM_014709.3 N2094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr2:61633156 G>A maps to NM_014709.3 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr11:77917030 C>G maps to NM_020798.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr11:77907405 C>T maps to NM_020798.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr11:77921372 G>T maps to NM_020798.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2298-01A-01W-0799-08 chr17:76799702 G>A maps to NM_025090.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr2:219324533 C>T maps to NM_020935.2 E874E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr7:6182630 G>C maps to ENST00000404835 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr17:9631298 G>T maps to NM_153210.3 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr6:99894074 C>A maps to NM_001080481.1 G525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr11:11964114 G>A maps to ENST00000399455 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr23:55513443 C>T did not map to a codon.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr23:55514318 T>C did not map to a codon.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr10:75276829 A>G maps to NM_152586.3 Y1118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1687-01A-01W-0633-09 chr17:5072321 C>A maps to NM_004505.2 L1163L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-23-1124-01A-01W-0488-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr16:8988938 G>A maps to NM_003470.2 H996H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr15:50769602 G>A maps to NM_005154.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr23:40988341 T>A did not map to a codon.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:40990732 T>G did not map to a codon.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr23:41000576 A>G did not map to a codon.
Sequencing variant TCGA-61-1995-01A-01W-0722-08 chr23:41075554 A>G did not map to a codon.
Sequencing variant TCGA-20-0990-01A-01W-0486-08 chr23:129054484 G>T did not map to a codon.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr23:129063582 G>C did not map to a codon.
Sequencing variant TCGA-25-2393-01A-01W-0799-08 chr13:52604307 C>T maps to NM_021645.5 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr12:101757448 C>G maps to NM_014503.2 Y1962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr6:144759886 C>T maps to NM_007124.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr14:77237583 G>C maps to NM_014909.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr19:6828899 C>G maps to NM_005428.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1120-01A-02W-0484-10 chr1:108298099 A>G maps to NM_006113.4 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1103-01A-01W-0488-09 chr1:108313292 C>A maps to NM_006113.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr1:108299881 C>G did not map to a codon.
Sequencing variant TCGA-25-1320-01A-01W-0492-08 chr1:108311107 T>C maps to NM_006113.4 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr10:118895991 G>A maps to NM_001112704.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1696-01A-01W-0633-09 chr1:101190291 G>A maps to NM_001078.3 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr5:82785989 G>A maps to NM_004385.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2056-01B-01W-0722-08 chr5:82835616 T>C maps to NM_004385.4 T2265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr5:82836624 A>C maps to NM_004385.4 V2601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2288-01A-01W-0799-08 chr5:82834548 A>G maps to NM_004385.4 S1909S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr5:82816311 T>C maps to NM_004385.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:7811258 G>C did not map to a codon.
Sequencing variant TCGA-09-1675-01B-01W-0633-09 chr23:8434366 C>T did not map to a codon.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr12:48251310 G>C maps to NM_001017535.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr10:135053309 G>A maps to NM_014468.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr3:156979051 G>A maps to NM_001167912.1 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1562-01A-01W-0553-09 chr17:56056654 G>A maps to NM_007146.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr23:135630948 C>T did not map to a codon.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr23:135631121 G>A did not map to a codon.
Sequencing variant TCGA-23-1030-01A-02W-0486-08 chr3:11643367 C>A maps to NM_014667.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr2:219293014 C>T maps to NM_007127.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr2:37010537 A>G maps to NM_053276.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1727-01A-01W-0639-09 chr23:150572159 G>A did not map to a codon.
Sequencing variant TCGA-13-0807-01B-02W-0421-09 chr19:53770597 G>T maps to NM_173857.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr1:247420026 C>T maps to NM_173858.1 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr6:133004389 C>T maps to NM_004666.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr6:133004363 G>C maps to NM_004666.2 S486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr6:133072586 A>G maps to NM_004665.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr3:51458101 G>A maps to ENST00000273612 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr9:79984212 A>G did not map to a codon.
Sequencing variant TCGA-29-2434-01A-01D-1526-09 chr9:79981665 T>C maps to ENST00000376646 S2784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr8:100479762 T>A maps to NM_017890.3 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr8:100791075 A>G maps to NM_017890.3 L2557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1703-01A-01W-0633-09 chr8:100847944 C>T maps to NM_017890.3 D3332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr8:100133433 C>T maps to NM_017890.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr15:62201252 C>T maps to NM_020821.2 E2972E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1914-01A-01W-0639-09 chr15:62257012 G>A maps to NM_020821.2 V1033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr1:12333151 T>A maps to NM_015378.2 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr1:12557551 A>G did not map to a codon.
Sequencing variant TCGA-29-1769-01A-01W-0639-09 chr1:12409305 C>G maps to NM_015378.2 P3102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2095-01A-01W-0722-08 chr1:12475240 C>T maps to NM_015378.2 F4044F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr15:41191654 C>T maps to NM_020857.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1556-01A-01W-0615-10 chr12:122745827 C>A maps to NM_022916.4 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr15:91548134 G>C maps to NM_018668.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr6:33236314 G>A maps to NM_022553.4 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr6:33238020 C>A maps to NM_022553.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1698-01A-01W-0633-09 chr17:559154 G>A maps to NM_001128159.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr23:107310216 C>G did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr11:124618353 G>A maps to NM_014312.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:65253584 C>G did not map to a codon.
Sequencing variant TCGA-13-0905-01B-01W-0492-08 chr7:54617630 C>A maps to ENST00000404951 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2552-01A-01D-1526-09 chr7:54612402 G>A maps to ENST00000404951 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr17:26695998 G>C maps to NM_000638.3 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr2:98804463 A>C maps to NM_144992.4 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2354-01A-01W-0799-08 chr2:98920175 T>A maps to NM_144992.4 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2042-01A-01W-0799-08 chr11:123989725 C>G maps to NM_014622.4 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr11:61053804 G>T maps to NM_152718.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1424-01A-01W-0549-09 chr11:61041991 C>T maps to NM_152718.2 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1356-01A-01W-0492-08 chr12:6128551 G>A maps to NM_000552.3 A1344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr12:6184516 G>A maps to NM_000552.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr12:6062761 T>G did not map to a codon.
Sequencing variant TCGA-23-1117-01A-02W-0488-09 chr12:6167144 G>A maps to NM_000552.3 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1761-01A-01W-0633-09 chr12:6094774 G>A maps to NM_000552.3 S2285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0890-01A-01W-0421-09 chr10:28900851 G>T did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr14:100809635 G>T maps to NM_173701.1 C305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1686-01A-01W-0633-09 chr23:48544182 G>A did not map to a codon.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr23:48547365 C>T did not map to a codon.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr1:27755385 C>T maps to NM_006990.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr12:14946677 T>C maps to NM_016312.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr23:48458029 G>A did not map to a codon.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr23:48457118 G>A did not map to a codon.
Sequencing variant TCGA-25-1630-01A-01W-0615-10 chr23:48457321 C>T did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:48460327 T>C did not map to a codon.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr23:48463353 C>T did not map to a codon.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr17:9536211 C>T maps to NM_145054.4 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr17:9538753 G>A maps to NM_145054.4 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2012-01A-01W-0722-08 chr4:177089797 G>T did not map to a codon.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr16:739274 C>T maps to ENST00000248142 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr1:224607295 T>G maps to NM_025160.6 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2008-01A-02W-0722-08 chr6:170059615 T>G did not map to a codon.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr9:116082735 A>C maps to NM_001012361.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr2:128525785 T>A maps to NM_018383.4 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr2:20138093 T>A maps to NM_001006657.1 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1699-01A-01W-0633-09 chr10:1170848 G>A did not map to a codon.
Sequencing variant TCGA-23-2072-01A-01W-0722-08 chr23:117527020 G>A did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr23:48933302 G>T did not map to a codon.
Sequencing variant TCGA-13-1489-01A-01W-0549-09 chr17:80574439 C>A maps to NM_019613.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr3:39093554 G>A maps to NM_020839.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1672-01A-01W-0633-09 chr3:167223146 G>A maps to NM_178824.3 C592C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1114-01B-01W-0633-09 chr3:49052720 A>C maps to NM_018031.3 *1152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr7:158711560 G>T did not map to a codon.
Sequencing variant TCGA-61-1895-01A-01W-0639-09 chr15:78575863 C>T did not map to a codon.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr1:43675632 C>T maps to NM_152498.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr12:122369782 C>A maps to NM_144668.4 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr12:122359528 C>A maps to NM_144668.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1674-01A-01W-0633-09 chr2:228769697 C>A maps to NM_178821.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1628-01A-01W-0615-10 chr18:54603084 G>A maps to NM_015285.2 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr11:62607021 G>C maps to NM_018093.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr1:67337150 A>C maps to NM_024763.4 L281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr14:64065624 A>G maps to NM_080666.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr15:90276308 C>A maps to NM_020212.1 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1711-01A-01W-0633-09 chr8:124440175 T>A maps to NM_018024.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1407-01A-01W-0490-10 chr11:9598751 A>G maps to NM_003390.3 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr20:43752883 G>A maps to NM_080869.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr20:43739360 G>A maps to ENST00000307971 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr15:83499812 G>T maps to NM_001080435.1 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr15:83502191 G>A maps to NM_001080435.1 E778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-0369-01A-01W-0372-09 chr4:1980537 A>C maps to NM_133335.3 R1334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr8:38146955 C>T maps to NM_023034.1 E1062E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr12:65471524 C>T did not map to a codon.
Sequencing variant TCGA-09-2053-01C-01W-0722-08 chr2:175436887 G>A maps to NM_003387.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr17:38416785 G>A did not map to a codon.
Sequencing variant TCGA-31-1953-01A-01W-0699-08 chr7:5257578 C>T maps to NM_015610.3 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1766-01A-01W-0633-09 chr19:15559001 C>A maps to ENST00000389282 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr12:977828 A>G maps to NM_001184985.1 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr12:939280 C>T maps to NM_001184985.1 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1498-01A-01W-0549-09 chr12:988773 C>A maps to NM_018979.3 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1369-01A-02D-1526-09 chr23:54278101 G>A did not map to a codon.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr23:54319580 G>C did not map to a codon.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr23:54275417 G>T did not map to a codon.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr23:54321212 G>A did not map to a codon.
Sequencing variant TCGA-61-2002-01A-01W-0722-08 chr23:54259358 G>A did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr17:40939862 G>A maps to NM_032387.4 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr7:116937750 A>T maps to NM_003391.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2088-01A-01W-0722-08 chr7:116955205 G>A maps to NM_003391.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1348-01A-01W-0494-09 chr1:228210472 C>T maps to ENST00000366753 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1683-01A-01W-0633-09 chr3:55504323 C>T maps to NM_003392.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr22:46327178 G>A maps to NM_058238.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1032-01A-02W-0486-08 chr12:118472045 T>C maps to ENST00000441406 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2612-01A-01W-1092-09 chr17:6023695 C>T maps to NM_015253.1 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1919-01A-01W-0699-08 chr12:108641999 C>T maps to ENST00000261400 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr5:167894879 G>A maps to NM_001161661.1 Q1068Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr4:184190298 C>T maps to ENST00000448232 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr23:10035468 C>T did not map to a codon.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr23:10062213 G>A did not map to a codon.
Sequencing variant TCGA-23-2078-01A-01W-0722-08 chr23:10084546 G>T did not map to a codon.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr23:10085307 C>G did not map to a codon.
Sequencing variant TCGA-42-2582-01A-01D-1526-09 chr23:10085347 C>T did not map to a codon.
Sequencing variant TCGA-23-2647-01A-01D-1526-09 chr3:149290702 G>A maps to NM_001168278.1 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr23:52844154 C>A did not map to a codon.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr3:46062719 G>A maps to NM_005283.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr2:31588861 T>A maps to NM_000379.3 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr23:2729382 T>C did not map to a codon.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr23:123040921 T>A did not map to a codon.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr23:123020044 A>G did not map to a codon.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr23:123034351 T>C did not map to a codon.
Sequencing variant TCGA-42-2591-01A-01D-1526-09 chr23:123040872 G>C did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr3:39225422 G>A maps to NM_194293.2 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr3:39227279 G>A maps to NM_194293.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2533-01A-01D-1526-09 chr3:39225776 C>T maps to NM_194293.2 G1720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr2:168104777 A>G maps to NM_152381.5 P2292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr2:168105326 G>C maps to NM_152381.5 T2475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr2:168100109 C>T maps to NM_152381.5 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0795-01A-01W-0372-09 chr20:30585010 C>T maps to NM_001011718.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr8:71646496 T>C maps to NM_001011720.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr23:100169656 G>T did not map to a codon.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr23:100169626 G>A did not map to a codon.
Sequencing variant TCGA-13-0804-01A-01W-0372-09 chr10:111628445 G>A maps to NM_020383.3 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr10:111624956 G>A maps to NM_020383.3 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr23:128901658 T>C did not map to a codon.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr2:61724138 G>A maps to NM_003400.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0991-01A-03D-0428-08 chr16:28115941 G>A maps to NM_015171.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1781-01A-01W-0633-09 chr16:28167687 T>A maps to NM_015171.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2024-01A-02W-0722-08 chr12:64827255 G>C maps to NM_007235.3 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr1:180793949 C>G maps to NM_004736.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr19:44065142 C>T maps to NM_006297.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1582-01A-01W-0615-10 chr19:44051128 C>T maps to NM_006297.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr19:44050048 C>G maps to NM_006297.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr12:58340807 C>T maps to NM_033276.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1567-01A-01W-0615-10 chr20:21336788 G>T maps to NM_012255.3 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr11:74556115 A>G did not map to a codon.
Sequencing variant TCGA-36-2530-01A-01D-1526-09 chr11:74632353 G>C maps to NM_182969.1 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr1:43166658 C>T maps to NM_004559.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1357-01A-01W-0492-08 chr3:183442220 T>A maps to NM_018023.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr18:724572 G>A maps to NM_005433.3 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1514-01A-01W-0552-10 chr1:54332040 G>A maps to NM_018982.4 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr23:67731780 G>C did not map to a codon.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr14:75287833 C>T maps to NM_019589.2 S2035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr2:135738767 A>T maps to NM_025052.3 C1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1319-01A-01W-0492-08 chr4:69184445 G>A maps to NM_001031732.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr17:1303361 C>A maps to NM_006761.4 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1434-01A-01W-0545-08 chr7:100364275 C>T maps to ENST00000349350 G1533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1904-01A-01W-0639-09 chr7:100369561 C>T maps to ENST00000349350 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr3:167016201 T>C maps to ENST00000307529 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr23:2407123 T>A did not map to a codon.
Sequencing variant TCGA-13-1412-01A-01W-0494-09 chr20:56191345 A>C maps to NM_030776.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr8:81430805 G>A maps to NM_001105539.1 W710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1635-01A-01W-0615-10 chr3:101370392 G>A maps to NM_014415.3 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0927-01A-02W-0419-10 chr11:113934216 C>T maps to NM_001018011.1 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr3:114069697 G>A maps to NM_001164342.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1343-01A-01W-0488-09 chr6:33284545 G>A maps to NM_001145338.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr6:33282986 C>T maps to NM_001145338.1 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr6:109796644 G>A maps to NM_014797.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr11:62519927 C>T maps to NM_024784.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr23:119388044 A>G did not map to a codon.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr1:173842706 A>G maps to NM_032522.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2590-01A-01D-1526-09 chr12:57398677 T>C maps to NM_014830.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr17:7366383 G>A maps to NM_020899.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr9:129596149 C>T maps to NM_014007.3 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr20:62421515 C>A maps to NM_025224.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr20:62422005 C>A maps to NM_025224.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1857-01A-02W-0639-09 chr9:37442074 G>C maps to NM_014872.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1770-01A-01W-0633-09 chr11:110035369 C>G maps to NM_033390.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-1568-01A-01W-0615-10 chr13:46619618 G>A maps to ENST00000242848 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr19:47597798 G>A maps to NM_015168.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-57-1993-01A-01W-0699-08 chr19:47570524 C>T maps to NM_015168.1 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr2:113080461 G>A maps to NM_198581.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1324-01A-01W-0490-10 chr22:41735145 C>G maps to ENST00000351589 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1662-01A-01W-0615-10 chr7:138732461 G>A maps to ENST00000464606 Q985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr23:64141802 G>A did not map to a codon.
Sequencing variant TCGA-13-1405-01A-01W-0494-09 chr1:52941172 G>A maps to NM_001009881.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1855-01A-01W-0639-09 chr1:52991499 T>C maps to NM_001009881.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr23:117959653 G>A did not map to a codon.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr23:111698392 C>T did not map to a codon.
Sequencing variant TCGA-36-2532-01A-01D-1526-09 chr23:111698665 C>T did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr23:103359002 A>T did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr23:103359503 G>T did not map to a codon.
Sequencing variant TCGA-23-1031-01A-01W-0486-08 chr23:77913138 C>G did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr9:88937964 G>T maps to NM_024617.3 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr12:122966490 C>G did not map to a codon.
Sequencing variant TCGA-29-1778-01A-01W-0639-09 chr12:122958436 C>T maps to NM_017612.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1652-01A-01W-0639-09 chr7:100013926 C>T did not map to a codon.
Sequencing variant TCGA-24-1551-01A-01W-0551-08 chr3:28454756 A>G maps to NM_001040432.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2009-01A-01W-0722-08 chr2:207169947 T>C maps to NM_020923.1 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1331-01A-01W-0486-08 chr23:74742741 C>T did not map to a codon.
Sequencing variant TCGA-23-2645-01A-01W-1091-09 chr23:74636972 G>C did not map to a codon.
Sequencing variant TCGA-24-2261-01A-01W-0722-08 chr23:74649786 G>A did not map to a codon.
Sequencing variant TCGA-24-1564-01A-01W-0551-08 chr10:99212185 C>T maps to NM_198046.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1427-01A-01W-0549-09 chr3:195938077 G>A maps to NM_001039617.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr3:113675208 C>G maps to NM_173570.3 S299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0792-01A-01W-0370-10 chr11:66311274 G>T maps to NM_207340.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2071-01A-02D-1526-09 chr3:44968336 T>A maps to NM_016598.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1555-01A-01W-0552-10 chr23:128957687 C>T did not map to a codon.
Sequencing variant TCGA-13-0883-01A-02W-0420-08 chr10:31809759 T>C maps to NM_001174096.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr10:31810578 C>T maps to NM_001174096.1 C773C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1423-01A-01W-0545-08 chr2:145147302 C>A maps to NM_014795.3 G1120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0937-01A-02W-0419-10 chr9:131516171 C>T maps to NM_006336.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1321-01A-01W-0492-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr6:38084453 G>T maps to NM_021943.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1365-01A-01W-0490-10 chr16:72992267 C>A maps to NM_006885.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0919-01A-01W-0419-10 chr16:72991599 C>G maps to NM_006885.3 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2065-01A-01D-1526-09 chr16:72822427 C>A maps to NM_006885.3 G3249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0931-01A-01W-0420-08 chr8:77766495 C>T maps to NM_024721.4 Q2447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr8:77768156 C>T maps to NM_024721.4 G3000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1504-01A-01W-0545-08 chr8:77766281 C>T maps to NM_024721.4 N2375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr8:77761833 G>T maps to NM_024721.4 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1614-01A-01W-0552-10 chr8:77766446 A>G maps to NM_024721.4 P2430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1771-01A-01W-0633-09 chr8:77763428 G>A maps to NM_024721.4 A1424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2050-01A-01W-0799-08 chr19:44831843 T>C maps to ENST00000412927 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1843-01A-01W-0639-09 chr19:36851340 G>A maps to NM_020917.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr19:36832292 A>G maps to NM_020917.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr14:69259625 G>A maps to NM_004926.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1317-01A-01W-0490-10 chr14:69259622 G>A maps to NM_004926.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0938-01A-02W-0419-10 chr8:144332450 G>A maps to NM_173832.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr6:29640708 A>G maps to NM_001109809.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0899-01A-01W-0420-08 chr6:29641001 T>G maps to NM_001109809.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr6:29640603 G>A maps to NM_001109809.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr6:29641479 A>T maps to NM_001109809.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1847-01A-01W-0633-09 chr8:106811144 A>C maps to NM_012082.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1777-01A-01W-0639-09 chr8:106814619 T>A maps to NM_012082.3 C770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0935-01A-03W-0421-09 chr23:24226375 G>A did not map to a codon.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr23:24226334 A>G did not map to a codon.
Sequencing variant TCGA-13-0720-01A-01W-0370-10 chr14:73442335 C>A maps to NM_021260.2 G577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-2049-01D-01W-0799-08 chr14:68264944 A>G maps to NM_015346.3 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr14:68260426 C>T maps to NM_015346.3 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2060-01A-01W-0799-08 chr14:68274136 C>T maps to NM_015346.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-2427-01A-01W-0799-08 chr14:68252855 A>C maps to NM_015346.3 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1906-01A-01W-0639-09 chr1:52747333 T>A maps to NM_004799.2 Y957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr8:124267210 C>A maps to NM_007222.3 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr3:147128702 T>C maps to NM_003412.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr23:136651154 C>T did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr23:136649868 C>G did not map to a codon.
Sequencing variant TCGA-13-1488-01A-01W-0549-09 chr19:57286126 G>A maps to NM_001146326.1 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1563-01A-01W-0553-09 chr16:25255568 C>T maps to NM_001012981.4 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr16:25258424 A>C maps to NM_001012981.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1850-01A-01W-0639-09 chr6:28213600 G>A maps to NM_019110.3 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr23:101152945 G>A did not map to a codon.
Sequencing variant TCGA-24-2019-01A-02W-0722-08 chr23:101152860 G>A did not map to a codon.
Sequencing variant TCGA-24-2289-01A-01W-0799-08 chr23:101138611 C>T did not map to a codon.
Sequencing variant TCGA-13-1481-01A-01W-0549-09 chr10:81064922 C>A maps to NM_020338.3 C763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2551-01A-01D-1526-09 chr10:81070808 G>A maps to NM_020338.3 Q988Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1408-01A-01W-0490-10 chr7:44804073 T>A maps to NM_031449.3 C639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr7:44804966 G>A maps to NM_031449.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1491-01A-01W-0549-09 chr13:20641010 A>G maps to NM_001190965.1 V1051V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1915-01A-01W-0639-09 chr13:20567973 T>C maps to NM_001190965.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2404-01A-01W-0799-08 chr23:70465871 G>T did not map to a codon.
Sequencing variant TCGA-42-2589-01A-01D-1526-09 chr23:70472828 G>C did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr1:35480423 T>C maps to NM_007167.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2534-01A-01D-1526-09 chr17:4645730 A>T maps to NM_001136046.1 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1435-01A-01W-0549-09 chr10:75185962 C>T maps to NM_001024593.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr20:45891161 G>A maps to ENST00000471951 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr19:19790529 T>A maps to NM_033204.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2372-01A-01D-1526-09 chr7:64167242 C>T maps to NM_016220.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1907-01A-01W-0639-09 chr7:64438577 A>C maps to NM_015852.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0893-01B-01W-0494-09 chr7:6736968 C>A did not map to a codon.
Sequencing variant TCGA-24-1431-01A-01D-0472-08 chr19:9677500 G>C maps to NM_001008727.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0904-01A-02W-0420-08 chr20:18297067 C>A maps to ENST00000401790 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2035-01A-01W-0722-08 chr19:58579391 C>T maps to NM_007134.1 R538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr19:19824900 T>G maps to NM_021030.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2088-01A-01W-0722-08 chr12:133659686 A>C did not map to a codon.
Sequencing variant TCGA-24-2267-01A-01W-0799-08 chr2:219509558 C>G maps to NM_001105537.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1104-01A-01W-0488-09 chr8:146157868 G>A maps to NM_006958.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1403-01A-01W-0494-09 chr3:44612516 G>T maps to NM_018651.2 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr17:11894351 T>G maps to NM_144680.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1497-01A-01W-0549-09 chr23:47836154 T>C did not map to a codon.
Sequencing variant TCGA-23-1123-01A-01W-0488-09 chr23:47836715 G>A did not map to a codon.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr23:47842382 C>T did not map to a codon.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr6:27419768 A>C maps to NM_007149.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr23:152089283 C>T did not map to a codon.
Sequencing variant TCGA-24-1436-01A-01W-0549-09 chr23:152138984 A>G did not map to a codon.
Sequencing variant TCGA-61-2110-01A-01W-0722-08 chr23:152113971 C>A did not map to a codon.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr9:104170970 A>G maps to NM_003452.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1901-01A-01W-0639-09 chr19:12244148 C>T maps to NM_021143.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1549-01A-01W-0553-09 chr19:22155078 A>G maps to NM_007153.3 C919C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr7:148951469 G>A maps to NM_012256.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr20:52198015 G>A maps to NM_006526.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1362-01A-01W-0494-09 chr19:44934172 T>C maps to NM_014518.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr19:44933590 G>A maps to NM_014518.2 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1326-01A-01W-0492-08 chr17:5009792 C>A maps to NM_014519.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2544-01A-01D-1526-09 chr17:5009609 G>A maps to NM_014519.2 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1499-01A-01W-0549-09 chr18:74563807 G>A maps to NM_007345.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1718-01A-01W-0633-09 chr10:44053446 A>G maps to NM_001099284.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0894-01B-01W-0494-09 chr10:38126602 G>A maps to NM_021045.1 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1911-01A-01W-0639-09 chr10:38246346 C>A did not map to a codon.
Sequencing variant TCGA-36-2538-01A-01D-1526-09 chr19:58452730 C>T maps to NM_005773.2 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2539-01A-01D-1526-09 chr11:116655119 C>A maps to NM_003904.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1124-01A-01W-0488-09 chr16:3334003 C>T maps to NM_005741.4 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2537-01A-01D-1526-09 chr19:57705352 G>C maps to NM_003417.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1410-01A-01W-0492-08 chr19:58724490 G>A maps to NM_133502.1 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1404-01A-01W-0494-09 chr23:152612476 C>A did not map to a codon.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr23:152612700 C>T did not map to a codon.
Sequencing variant TCGA-23-2649-01A-01D-1526-09 chr16:89789686 C>T maps to NM_001113525.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr22:22843282 T>C maps to NM_080764.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2348-01A-01W-0799-08 chr22:22843711 T>C maps to NM_080764.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2113-01A-01W-0722-08 chr22:22842613 C>T maps to NM_080764.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr23:129377603 G>A did not map to a codon.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr19:44352483 G>A maps to NM_181845.1 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1422-01A-01W-0545-08 chr6:87965017 A>G maps to NM_015021.1 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1846-01A-01W-0639-09 chr21:43411519 T>A maps to NM_020727.4 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1737-01A-01W-0639-09 chr7:99669551 G>A maps to NM_032924.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0793-01A-01W-0370-10 chr6:28294631 C>T did not map to a codon.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr19:58967204 G>C maps to NM_207395.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1496-01A-01W-0545-08 chr20:45130462 A>G maps to NM_018102.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr10:38344560 G>C maps to NM_006954.1 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1714-01A-02W-0633-09 chr5:71739939 G>T maps to NM_152625.1 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr2:180634383 G>A maps to NM_152520.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1347-01A-01W-0488-09 chr7:148851128 A>G maps to NM_170686.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1809-01A-01W-0633-09 chr19:44377030 T>C maps to ENST00000324394 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr18:72343935 C>T maps to NM_017757.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr23:47307996 C>A did not map to a codon.
Sequencing variant TCGA-13-1505-01A-01D-0472-08 chr23:47307086 A>G did not map to a codon.
Sequencing variant TCGA-36-1570-01A-01W-0615-10 chr23:47308222 C>T did not map to a codon.
Sequencing variant TCGA-61-1903-01A-01W-0639-09 chr23:47308563 G>T did not map to a codon.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr19:58439071 A>T maps to NM_133460.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1899-01A-01W-0639-09 chr16:49764714 G>A maps to NM_015069.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr16:49823410 G>A maps to NM_015069.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr19:21991431 A>G maps to NM_003423.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1545-01A-01W-0615-10 chr19:52543794 G>A maps to ENST00000391795 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2092-01A-01W-0722-08 chr19:11892138 T>C maps to NM_152355.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0727-01A-01W-0370-10 chr3:44492425 A>G maps to NM_181489.5 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1413-01A-01W-0494-09 chr19:58988590 A>G maps to NM_017908.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0761-01A-01W-0370-10 chr23:134494390 A>T did not map to a codon.
Sequencing variant TCGA-23-1021-01B-01W-0488-09 chr23:134493887 C>A did not map to a codon.
Sequencing variant TCGA-36-2545-01A-01D-1526-09 chr23:134494199 A>G did not map to a codon.
Sequencing variant TCGA-13-1483-01A-01W-0549-09 chr9:109689720 G>A maps to NM_021224.4 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr9:109689186 T>C maps to NM_021224.4 G998G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1544-01A-01W-0615-10 chr9:109687140 C>T maps to NM_021224.4 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0886-01A-01W-0420-08 chr19:57037055 G>A maps to NM_020813.2 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1495-01A-01W-0545-08 chr19:50549779 C>T maps to NM_015428.1 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1702-01A-01W-0633-09 chr7:57188818 C>T maps to NM_033273.1 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr7:99219045 C>T maps to NM_145115.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2066-01A-01D-1526-09 chr3:44763286 C>T maps to NM_033210.4 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1367-01A-01W-0492-08 chr10:77158575 T>G maps to NM_032772.4 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-0987-01A-02W-0486-08 chr19:32844299 C>T maps to NM_014910.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1763-01A-02W-0633-09 chr10:97916760 A>T maps to NM_014803.3 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1338-01A-01W-0484-10 chr4:10445168 A>C maps to NM_053042.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr18:22806156 A>T maps to NM_015461.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr18:22805703 G>A maps to NM_015461.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2548-01A-01D-1526-09 chr19:58117972 T>C maps to NM_020880.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1364-01A-01W-0490-10 chr19:31025799 G>A maps to NM_014717.1 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1411-01A-01W-0494-09 chr19:31038886 C>T maps to NM_014717.1 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1466-01A-01W-0545-08 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1784-01A-02W-0633-09 chr19:30934606 C>A maps to NM_014717.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1995-01A-01W-0722-08 chr19:57910959 C>T maps to NM_001172773.1 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1740-01A-01W-0639-09 chr19:58049640 G>T maps to ENST00000376233 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0724-01A-01W-0372-09 chr19:7083613 C>T maps to NM_024341.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2262-01A-01W-0799-08 chr19:12638452 G>A maps to NM_144976.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr19:37440551 C>A maps to NM_198539.2 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1722-01A-01D-1556-09 chr19:38056087 G>A maps to NM_016536.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0755-01A-01W-0372-09 chr19:37643246 C>T maps to ENST00000356958 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr19:58290194 A>G maps to NM_017652.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1844-01A-01W-0639-09 chr19:58361423 G>A maps to NM_032828.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0765-01A-01W-0372-09 chr15:85327687 C>T maps to NM_014630.2 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1507-01A-01W-0549-09 chr15:85342396 C>T maps to NM_014630.2 H1031H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1762-01A-01W-0633-09 chr15:85341675 C>T maps to NM_014630.2 Q903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2352-01A-01W-0799-08 chr17:5086300 T>A maps to NM_032530.1 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1688-01A-01W-0633-09 chr15:64792019 G>A maps to NM_015042.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0930-01A-02W-0421-09 chr19:52856963 C>T maps to NM_001161425.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2398-01A-01W-0799-08 chr19:53208486 T>A maps to NM_001161500.1 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr19:52448888 T>C maps to NM_001031721.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1710-01A-02W-0633-09 chr19:52448710 A>G maps to NM_001031721.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr19:52520434 G>C maps to NM_025040.3 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-2030-01A-01W-0722-08 chr5:16451861 C>T maps to NM_033414.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1315-01A-01W-0494-09 chr17:16525649 G>A maps to NM_020787.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1842-01A-01W-0639-09 chr19:20807902 A>G maps to NM_001076675.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-09-1670-01A-01W-0633-09 chr19:11728200 C>T maps to NM_145295.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr23:47918465 T>C did not map to a codon.
Sequencing variant TCGA-36-1578-01A-01W-0615-10 chr23:47918884 C>A did not map to a codon.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr1:91404898 G>C maps to NM_201269.1 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1998-01A-01W-0722-08 chr1:91404918 T>A maps to NM_201269.1 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1856-01A-01W-0639-09 chr23:22291955 C>T did not map to a codon.
Sequencing variant TCGA-61-1913-01A-01W-0639-09 chr23:22291313 G>C did not map to a codon.
Sequencing variant TCGA-23-1118-01A-01W-0488-09 chr19:52400190 C>T maps to NM_023074.3 W19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1649-01A-01W-0639-09 chr19:11598599 C>T maps to NM_138783.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1693-01A-01W-0633-09 chr19:11609108 A>G did not map to a codon.
Sequencing variant TCGA-61-1910-01A-01W-0639-09 chr23:46332266 G>C did not map to a codon.
Sequencing variant TCGA-13-0800-01A-01W-0372-09 chr23:46360297 A>T did not map to a codon.
Sequencing variant TCGA-23-1029-01B-01W-0639-09 chr19:22363141 G>T maps to NM_001001411.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr1:120168564 C>T maps to NM_001080470.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0726-01A-01W-0372-09 chr8:146068279 T>C maps to ENST00000446747 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1417-01A-01W-0549-09 chr8:146062800 G>A maps to ENST00000446747 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2547-01A-01D-1526-09 chr22:24086676 G>A maps to NM_021916.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1651-01A-01W-0639-09 chr19:12060470 C>G maps to NM_144566.1 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1849-01A-01W-0639-09 chr19:53086334 T>C maps to NM_001172655.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-2641-01A-01D-1526-09 chr8:37553647 A>C maps to NM_025069.1 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1464-01A-01W-0549-09 chr8:102213846 G>T maps to NM_016096.3 C41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0910-01A-01W-0421-09 chr23:84519371 G>A did not map to a codon.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr23:84526276 C>A did not map to a codon.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr23:84526378 T>C did not map to a codon.
Alternatively spliced codon TCGA-13-0724-01A-01W-0372-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr7:55980377 G>T maps to NM_182633.1 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-10-0934-01A-02W-0420-08 chr19:21300345 T>A maps to NM_182515.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-04-1342-01A-01W-0486-08 chr4:436637 G>A maps to NM_133474.2 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-20-1682-01A-01W-0633-09 chr6:35259446 G>A maps to NM_003427.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1775-01A-01W-0639-09 chr6:35255570 T>C maps to NM_003427.3 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2102-01A-01W-0722-08 chr19:53958359 C>A maps to NM_001008401.3 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0885-01A-02W-0421-09 chr16:30567207 G>A maps to NM_033410.3 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1122-01A-01W-0486-08 chr19:53912238 G>T maps to NM_001040185.1 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1691-01A-01W-0633-09 chr19:52785428 T>A maps to NM_001010851.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1774-01A-01W-0639-09 chr19:2934296 G>T maps to NM_021217.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0906-01A-01W-0419-10 chr19:40541694 A>C maps to NM_001005851.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1024-01A-02W-0484-10 chr7:99081749 C>T maps to NM_213603.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-30-1891-01A-01W-0699-08 chr9:130198266 C>T maps to NM_007135.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1705-01A-01W-0633-09 chr3:113955597 C>T maps to NM_007136.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2613-01A-01W-1092-09 chr3:113955432 G>T maps to NM_007136.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0887-01A-01W-0421-09 chr2:185800653 T>A maps to NM_194250.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2400-01A-01W-0799-08 chr2:185800758 C>A maps to NM_194250.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1900-01A-01W-0639-09 chr2:185731239 G>C did not map to a codon.
Sequencing variant TCGA-13-0923-01A-01W-0420-08 chr7:88964350 C>A maps to NM_181646.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-2401-01A-01W-0799-08 chr7:88965091 A>G maps to NM_181646.2 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1482-01A-01W-0549-09 chr23:47774834 A>G did not map to a codon.
Sequencing variant TCGA-13-0912-01A-01W-0421-09 chr19:53994553 G>A maps to NM_001004301.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-42-2587-01A-01D-1526-09 chr19:53454172 G>T maps to NM_001031665.1 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-1733-01A-01W-0639-09 chr19:53454523 G>A maps to NM_001031665.1 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-31-1959-01A-01W-0699-08 chr16:71894400 G>T maps to ENST00000425432 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2097-01A-02W-0722-08 chr13:115090657 T>C maps to NM_032436.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-61-2101-01A-01W-0722-08 chr20:57782029 C>T maps to NM_178457.1 R1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1492-01A-01D-0472-08 chr14:102805456 G>A maps to NM_018335.3 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0791-01A-01W-0372-09 chr19:52569913 G>A maps to NM_001136499.1 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-36-2543-01A-01D-1526-09 chr19:52569724 T>C maps to NM_001136499.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr7:149545319 G>T maps to NM_001099220.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-23-1022-01A-02W-0488-09 chr19:20216090 T>A maps to NM_007138.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1463-01A-01W-0549-09 chr22:29445293 C>G maps to NM_032173.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2059-01A-01D-1526-09 chr16:21215389 G>C maps to NM_003460.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1484-01A-01W-0545-08 chr17:38029309 G>A maps to NM_199321.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr3:102187906 G>A maps to NM_175056.1 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-25-1329-01A-01W-0492-08 chr1:71532486 T>A maps to NM_203350.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0913-01A-01W-0420-08 chr19:58563898 A>T maps to NM_182572.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr15:85163857 G>C maps to NM_181877.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-24-1845-01A-01W-0639-09 chr1:33955117 G>T maps to NM_145238.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1509-01A-01W-0549-09 chr7:99661780 C>G maps to NM_145914.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr19:56733999 T>A maps to NM_024303.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0920-01A-01W-0421-09 chr19:56704058 A>G maps to NM_001080456.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-29-1701-01A-01W-0633-09 chr19:56701324 G>A maps to NM_001080456.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1409-01A-01W-0492-08 chr2:187713715 C>A maps to NM_182521.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-2057-01A-02D-1526-09 chr20:44486544 C>T maps to NM_080752.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-0762-01A-01W-0370-10 chr11:113610104 C>G did not map to a codon.
Sequencing variant TCGA-24-1474-01A-01W-0551-08 chr23:57935895 T>G did not map to a codon.
Sequencing variant TCGA-13-0760-01A-01W-0372-09 chr17:3920844 G>C maps to NM_015113.3 L2607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-13-1512-01A-01W-0545-08 chr1:78097566 T>C maps to NM_015534.4 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-59-2351-01A-01W-0799-08 chr1:78041806 A>G maps to NM_015534.4 D759D. Only missense variants will be evaluated by CHASM.
